X-linked retinoschisis with a novel substitutive amino acid (P193S) in XLRS1

Saved in:
Bibliographic Details
Published in:Human mutation 1999, Vol.13 (3), p.259-259
Main Authors: Duval, Pierre-André, Marlhens, Françoise, Griffoin, Jean-Michel, Millet, Pierre, Arnaud, Bernard, Hamel, Christian P.
Format: Article
Language:English
Subjects:
gene mutation
Müller cells
retinal dystrophy
X-linked retinoschisis
XLRS1
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by
cites
container_end_page 259
container_issue 3
container_start_page 259
container_title Human mutation
container_volume 13
creator Duval, Pierre-André
Marlhens, Françoise
Griffoin, Jean-Michel
Millet, Pierre
Arnaud, Bernard
Hamel, Christian P.
description
doi_str_mv 10.1002/(SICI)1098-1004(1999)13:3<259::AID-HUMU18>3.0.CO;2-W
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_197290691</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>781998931</sourcerecordid><originalsourceid>FETCH-LOGICAL-c2218-820dbb3ea25d6e07dbaf54f816efef0937e9320373ea4fb4840d8d703423d7853</originalsourceid><addsrcrecordid>eNp9kE1P20AQhi3USlDa_7DilBw2nf1wdjcgJDAtRHWbliSE28iO12Ih2NTrQPn3XcuIC1VP86F3npGeKDpiMGIA_PNgPk2mQwZG0zDLATPGDJmYiCMem8nkZHpGL5bfl0wfixGMktkhp6udaO_14F3Xx4YqZeRu9MH7WwDQcSz2ovSablx1ZwvS2NZVtV_fOO88eXLtDclIVT_aDfHb3Leu3bbu0ZLsPsRItnYFGfxkRsyHxFXkOr2cs4_R-zLbePvppe5Hy69fFskFTWfn0-QkpWvOmaaaQ5HnwmY8LsYWVJFnZSxLzca2tCUYoawRHIQKEVnmUksodKFASC4KpWOxHx303Iem_r21vsXbettU4SUyo7iBsWEhtOhD66b2vrElPjTuPmuekQF2WhE7rdhZ6maJnVZkAgUGrYhBK_ZawwYwmSHHVcBe9dgnt7HPb5j_Rf6T-LIJYNqDnW_tn1dw1tzhWAkV4-rHOZozuUh_sW94Kv4C_FGYGw</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>197290691</pqid></control><display><type>article</type><title>X-linked retinoschisis with a novel substitutive amino acid (P193S) in XLRS1</title><source>Publicly Available Content Database</source><creator>Duval, Pierre-André ; Marlhens, Françoise ; Griffoin, Jean-Michel ; Millet, Pierre ; Arnaud, Bernard ; Hamel, Christian P.</creator><creatorcontrib>Duval, Pierre-André ; Marlhens, Françoise ; Griffoin, Jean-Michel ; Millet, Pierre ; Arnaud, Bernard ; Hamel, Christian P.</creatorcontrib><identifier>ISSN: 1059-7794</identifier><identifier>EISSN: 1098-1004</identifier><identifier>DOI: 10.1002/(SICI)1098-1004(1999)13:3&lt;259::AID-HUMU18&gt;3.0.CO;2-W</identifier><language>eng</language><publisher>New York: John Wiley &amp; Sons, Inc</publisher><subject>gene mutation ; Müller cells ; retinal dystrophy ; X-linked retinoschisis ; XLRS1</subject><ispartof>Human mutation, 1999, Vol.13 (3), p.259-259</ispartof><rights>Copyright © 1999 Wiley‐Liss, Inc.</rights><rights>Copyright © 1999 Wiley-Liss, Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/197290691/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/197290691?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,4024,25753,27923,27924,27925,37012,44590,75126</link.rule.ids></links><search><creatorcontrib>Duval, Pierre-André</creatorcontrib><creatorcontrib>Marlhens, Françoise</creatorcontrib><creatorcontrib>Griffoin, Jean-Michel</creatorcontrib><creatorcontrib>Millet, Pierre</creatorcontrib><creatorcontrib>Arnaud, Bernard</creatorcontrib><creatorcontrib>Hamel, Christian P.</creatorcontrib><title>X-linked retinoschisis with a novel substitutive amino acid (P193S) in XLRS1</title><title>Human mutation</title><addtitle>Hum. Mutat</addtitle><subject>gene mutation</subject><subject>Müller cells</subject><subject>retinal dystrophy</subject><subject>X-linked retinoschisis</subject><subject>XLRS1</subject><issn>1059-7794</issn><issn>1098-1004</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNp9kE1P20AQhi3USlDa_7DilBw2nf1wdjcgJDAtRHWbliSE28iO12Ih2NTrQPn3XcuIC1VP86F3npGeKDpiMGIA_PNgPk2mQwZG0zDLATPGDJmYiCMem8nkZHpGL5bfl0wfixGMktkhp6udaO_14F3Xx4YqZeRu9MH7WwDQcSz2ovSablx1ZwvS2NZVtV_fOO88eXLtDclIVT_aDfHb3Leu3bbu0ZLsPsRItnYFGfxkRsyHxFXkOr2cs4_R-zLbePvppe5Hy69fFskFTWfn0-QkpWvOmaaaQ5HnwmY8LsYWVJFnZSxLzca2tCUYoawRHIQKEVnmUksodKFASC4KpWOxHx303Iem_r21vsXbettU4SUyo7iBsWEhtOhD66b2vrElPjTuPmuekQF2WhE7rdhZ6maJnVZkAgUGrYhBK_ZawwYwmSHHVcBe9dgnt7HPb5j_Rf6T-LIJYNqDnW_tn1dw1tzhWAkV4-rHOZozuUh_sW94Kv4C_FGYGw</recordid><startdate>1999</startdate><enddate>1999</enddate><creator>Duval, Pierre-André</creator><creator>Marlhens, Françoise</creator><creator>Griffoin, Jean-Michel</creator><creator>Millet, Pierre</creator><creator>Arnaud, Bernard</creator><creator>Hamel, Christian P.</creator><general>John Wiley &amp; Sons, Inc</general><general>Hindawi Limited</general><scope>BSCLL</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QP</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>P64</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>RC3</scope></search><sort><creationdate>1999</creationdate><title>X-linked retinoschisis with a novel substitutive amino acid (P193S) in XLRS1</title><author>Duval, Pierre-André ; Marlhens, Françoise ; Griffoin, Jean-Michel ; Millet, Pierre ; Arnaud, Bernard ; Hamel, Christian P.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2218-820dbb3ea25d6e07dbaf54f816efef0937e9320373ea4fb4840d8d703423d7853</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>gene mutation</topic><topic>Müller cells</topic><topic>retinal dystrophy</topic><topic>X-linked retinoschisis</topic><topic>XLRS1</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Duval, Pierre-André</creatorcontrib><creatorcontrib>Marlhens, Françoise</creatorcontrib><creatorcontrib>Griffoin, Jean-Michel</creatorcontrib><creatorcontrib>Millet, Pierre</creatorcontrib><creatorcontrib>Arnaud, Bernard</creatorcontrib><creatorcontrib>Hamel, Christian P.</creatorcontrib><collection>Istex</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest Biological Science Journals</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Genetics Abstracts</collection><jtitle>Human mutation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Duval, Pierre-André</au><au>Marlhens, Françoise</au><au>Griffoin, Jean-Michel</au><au>Millet, Pierre</au><au>Arnaud, Bernard</au><au>Hamel, Christian P.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>X-linked retinoschisis with a novel substitutive amino acid (P193S) in XLRS1</atitle><jtitle>Human mutation</jtitle><addtitle>Hum. Mutat</addtitle><date>1999</date><risdate>1999</risdate><volume>13</volume><issue>3</issue><spage>259</spage><epage>259</epage><pages>259-259</pages><issn>1059-7794</issn><eissn>1098-1004</eissn><cop>New York</cop><pub>John Wiley &amp; Sons, Inc</pub><doi>10.1002/(SICI)1098-1004(1999)13:3&lt;259::AID-HUMU18&gt;3.0.CO;2-W</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1059-7794
ispartof Human mutation, 1999, Vol.13 (3), p.259-259
issn 1059-7794
1098-1004
language eng
recordid cdi_proquest_journals_197290691
source Publicly Available Content Database
subjects gene mutation
Müller cells
retinal dystrophy
X-linked retinoschisis
XLRS1
title X-linked retinoschisis with a novel substitutive amino acid (P193S) in XLRS1
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-28T12%3A14%3A22IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=X-linked%20retinoschisis%20with%20a%20novel%20substitutive%20amino%20acid%20(P193S)%20in%20XLRS1&rft.jtitle=Human%20mutation&rft.au=Duval,%20Pierre-Andr%C3%A9&rft.date=1999&rft.volume=13&rft.issue=3&rft.spage=259&rft.epage=259&rft.pages=259-259&rft.issn=1059-7794&rft.eissn=1098-1004&rft_id=info:doi/10.1002/(SICI)1098-1004(1999)13:3%3C259::AID-HUMU18%3E3.0.CO;2-W&rft_dat=%3Cproquest_cross%3E781998931%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c2218-820dbb3ea25d6e07dbaf54f816efef0937e9320373ea4fb4840d8d703423d7853%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=197290691&rft_id=info:pmid/&rfr_iscdi=true