A novel KIF5a mutation identified in two-family members with spastic paraplegia type 10

Saved in:
Bibliographic Details
Published in:Revue neurologique 2021-01, Vol.177 (1-2), p.152-154
Main Authors: Oliveira, R., Maruta, C., Gil-Gouveia, R.
Format: Article
Language:English
Subjects:
Family
Humans
Kinesins - genetics
Mutation
Paraplegia - diagnosis
Paraplegia - genetics
Pedigree
Spastic Paraplegia, Hereditary - diagnosis
Spastic Paraplegia, Hereditary - genetics
Citations: Items that this one cites
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by
cites cdi_FETCH-LOGICAL-c311t-29f6dad5d6f2aafaef183eb44c3876886c2b5fb429c458611faff1b6d74d04d63
container_end_page 154
container_issue 1-2
container_start_page 152
container_title Revue neurologique
container_volume 177
creator Oliveira, R.
Maruta, C.
Gil-Gouveia, R.
description
doi_str_mv 10.1016/j.neurol.2020.04.026
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2467613592</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0035378720306081</els_id><sourcerecordid>2467613592</sourcerecordid><originalsourceid>FETCH-LOGICAL-c311t-29f6dad5d6f2aafaef183eb44c3876886c2b5fb429c458611faff1b6d74d04d63</originalsourceid><addsrcrecordid>eNp9kDtPwzAUhT2AKK9_gJBHlgS_4qQLUlVRQCCxgBgtx74GV3lhO1T996QqMDLd5Tvn6H4IXVCSU0Ll9TrvYAx9kzPCSE5ETpg8QMeE8CLjZVXO0EmMa0IYLQk_QjPOWckKKY7R2wJ3_Rc0-PFhVWjcjkkn33fYW-iSdx4s9h1Omz5zuvXNFrfQ1hAi3vj0geOgY_IGDzrooYF3r3HaDoApOUOHTjcRzn_uKXpd3b4s77On57uH5eIpM5zSlLG5k1bbwkrHtHYaHK041EIYXpWyqqRhdeFqweZGFJWk1GnnaC1tKSwRVvJTdLXvHUL_OUJMqvXRQNPoDvoxKiZkKSkv5mxCxR41oY8xgFND8K0OW0WJ2mlUa7XXqHYaFRFq0jjFLn8WxroF-xf6dTgBN3sApj-_PAQVjYfOgPUBTFK29_8vfAOmHYfz</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2467613592</pqid></control><display><type>article</type><title>A novel KIF5a mutation identified in two-family members with spastic paraplegia type 10</title><source>ScienceDirect Freedom Collection</source><creator>Oliveira, R. ; Maruta, C. ; Gil-Gouveia, R.</creator><creatorcontrib>Oliveira, R. ; Maruta, C. ; Gil-Gouveia, R.</creatorcontrib><identifier>ISSN: 0035-3787</identifier><identifier>DOI: 10.1016/j.neurol.2020.04.026</identifier><identifier>PMID: 33272564</identifier><language>eng</language><publisher>France: Elsevier Masson SAS</publisher><subject>Family ; Humans ; Kinesins - genetics ; Mutation ; Paraplegia - diagnosis ; Paraplegia - genetics ; Pedigree ; Spastic Paraplegia, Hereditary - diagnosis ; Spastic Paraplegia, Hereditary - genetics</subject><ispartof>Revue neurologique, 2021-01, Vol.177 (1-2), p.152-154</ispartof><rights>2020</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c311t-29f6dad5d6f2aafaef183eb44c3876886c2b5fb429c458611faff1b6d74d04d63</cites><orcidid>0000-0003-1181-1418</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33272564$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Oliveira, R.</creatorcontrib><creatorcontrib>Maruta, C.</creatorcontrib><creatorcontrib>Gil-Gouveia, R.</creatorcontrib><title>A novel KIF5a mutation identified in two-family members with spastic paraplegia type 10</title><title>Revue neurologique</title><addtitle>Rev Neurol (Paris)</addtitle><subject>Family</subject><subject>Humans</subject><subject>Kinesins - genetics</subject><subject>Mutation</subject><subject>Paraplegia - diagnosis</subject><subject>Paraplegia - genetics</subject><subject>Pedigree</subject><subject>Spastic Paraplegia, Hereditary - diagnosis</subject><subject>Spastic Paraplegia, Hereditary - genetics</subject><issn>0035-3787</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp9kDtPwzAUhT2AKK9_gJBHlgS_4qQLUlVRQCCxgBgtx74GV3lhO1T996QqMDLd5Tvn6H4IXVCSU0Ll9TrvYAx9kzPCSE5ETpg8QMeE8CLjZVXO0EmMa0IYLQk_QjPOWckKKY7R2wJ3_Rc0-PFhVWjcjkkn33fYW-iSdx4s9h1Omz5zuvXNFrfQ1hAi3vj0geOgY_IGDzrooYF3r3HaDoApOUOHTjcRzn_uKXpd3b4s77On57uH5eIpM5zSlLG5k1bbwkrHtHYaHK041EIYXpWyqqRhdeFqweZGFJWk1GnnaC1tKSwRVvJTdLXvHUL_OUJMqvXRQNPoDvoxKiZkKSkv5mxCxR41oY8xgFND8K0OW0WJ2mlUa7XXqHYaFRFq0jjFLn8WxroF-xf6dTgBN3sApj-_PAQVjYfOgPUBTFK29_8vfAOmHYfz</recordid><startdate>202101</startdate><enddate>202101</enddate><creator>Oliveira, R.</creator><creator>Maruta, C.</creator><creator>Gil-Gouveia, R.</creator><general>Elsevier Masson SAS</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-1181-1418</orcidid></search><sort><creationdate>202101</creationdate><title>A novel KIF5a mutation identified in two-family members with spastic paraplegia type 10</title><author>Oliveira, R. ; Maruta, C. ; Gil-Gouveia, R.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c311t-29f6dad5d6f2aafaef183eb44c3876886c2b5fb429c458611faff1b6d74d04d63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Family</topic><topic>Humans</topic><topic>Kinesins - genetics</topic><topic>Mutation</topic><topic>Paraplegia - diagnosis</topic><topic>Paraplegia - genetics</topic><topic>Pedigree</topic><topic>Spastic Paraplegia, Hereditary - diagnosis</topic><topic>Spastic Paraplegia, Hereditary - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Oliveira, R.</creatorcontrib><creatorcontrib>Maruta, C.</creatorcontrib><creatorcontrib>Gil-Gouveia, R.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Revue neurologique</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Oliveira, R.</au><au>Maruta, C.</au><au>Gil-Gouveia, R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A novel KIF5a mutation identified in two-family members with spastic paraplegia type 10</atitle><jtitle>Revue neurologique</jtitle><addtitle>Rev Neurol (Paris)</addtitle><date>2021-01</date><risdate>2021</risdate><volume>177</volume><issue>1-2</issue><spage>152</spage><epage>154</epage><pages>152-154</pages><issn>0035-3787</issn><cop>France</cop><pub>Elsevier Masson SAS</pub><pmid>33272564</pmid><doi>10.1016/j.neurol.2020.04.026</doi><tpages>3</tpages><orcidid>https://orcid.org/0000-0003-1181-1418</orcidid></addata></record>
fulltext fulltext
identifier ISSN: 0035-3787
ispartof Revue neurologique, 2021-01, Vol.177 (1-2), p.152-154
issn 0035-3787
language eng
recordid cdi_proquest_miscellaneous_2467613592
source ScienceDirect Freedom Collection
subjects Family
Humans
Kinesins - genetics
Mutation
Paraplegia - diagnosis
Paraplegia - genetics
Pedigree
Spastic Paraplegia, Hereditary - diagnosis
Spastic Paraplegia, Hereditary - genetics
title A novel KIF5a mutation identified in two-family members with spastic paraplegia type 10
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-28T02%3A29%3A42IST&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=A%20novel%20KIF5a%20mutation%20identified%20in%20two-family%20members%20with%20spastic%20paraplegia%20type%2010&rft.jtitle=Revue%20neurologique&rft.au=Oliveira,%20R.&rft.date=2021-01&rft.volume=177&rft.issue=1-2&rft.spage=152&rft.epage=154&rft.pages=152-154&rft.issn=0035-3787&rft_id=info:doi/10.1016/j.neurol.2020.04.026&rft_dat=%3Cproquest_cross%3E2467613592%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c311t-29f6dad5d6f2aafaef183eb44c3876886c2b5fb429c458611faff1b6d74d04d63%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2467613592&rft_id=info:pmid/33272564&rfr_iscdi=true