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5-Aminolevulinate synthase is at 3p21 and thus not the primary defect in X-linked sideroblastic anemia
The gene for 5-aminolevulinate synthase (ALAS) has been mapped to 3pter-3q13.2 by Southern blot hybridization analysis of a mouse/human hybrid cell panel. In situ hybridization maps the gene to 3p21, distal to the common fragile site at 3p14.2 (FRA3B). The mapping of this gene to an autosome makes i...
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Published in: | American journal of human genetics 1988-09, Vol.43 (3), p.331-335 |
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container_title | American journal of human genetics |
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creator | SUTHERLAND, G. R BAKER, E CALLEN, D. F HYLAND, V. J MAY, B. K BAWDEN, M. J HEALY, H. M BORTHWICK, I. A |
description | The gene for 5-aminolevulinate synthase (ALAS) has been mapped to 3pter-3q13.2 by Southern blot hybridization analysis of a mouse/human hybrid cell panel. In situ hybridization maps the gene to 3p21, distal to the common fragile site at 3p14.2 (FRA3B). The mapping of this gene to an autosome makes it improbable that it is the site of the primary defect in X-linked sideroblastic anemia. |
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R ; BAKER, E ; CALLEN, D. F ; HYLAND, V. J ; MAY, B. K ; BAWDEN, M. J ; HEALY, H. M ; BORTHWICK, I. A</creator><creatorcontrib>SUTHERLAND, G. R ; BAKER, E ; CALLEN, D. F ; HYLAND, V. J ; MAY, B. K ; BAWDEN, M. J ; HEALY, H. M ; BORTHWICK, I. A</creatorcontrib><description>The gene for 5-aminolevulinate synthase (ALAS) has been mapped to 3pter-3q13.2 by Southern blot hybridization analysis of a mouse/human hybrid cell panel. In situ hybridization maps the gene to 3p21, distal to the common fragile site at 3p14.2 (FRA3B). The mapping of this gene to an autosome makes it improbable that it is the site of the primary defect in X-linked sideroblastic anemia.</description><identifier>ISSN: 0002-9297</identifier><identifier>EISSN: 1537-6605</identifier><identifier>PMID: 3414687</identifier><identifier>CODEN: AJHGAG</identifier><language>eng</language><publisher>Chicago, IL: University of Chicago Press</publisher><subject>5-Aminolevulinate Synthetase - genetics ; Anemia, Sideroblastic - genetics ; Anemias. Hemoglobinopathies ; Biological and medical sciences ; Chromosome Mapping ; Chromosomes, Human, Pair 3 ; Cloning, Molecular ; Defects ; Diseases of red blood cells ; Hematologic and hematopoietic diseases ; Humans ; Medical sciences ; Nucleic Acid Hybridization</subject><ispartof>American journal of human genetics, 1988-09, Vol.43 (3), p.331-335</ispartof><rights>1990 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1715374/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1715374/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,33223,53790,53792</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=6887954$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/3414687$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>SUTHERLAND, G. R</creatorcontrib><creatorcontrib>BAKER, E</creatorcontrib><creatorcontrib>CALLEN, D. F</creatorcontrib><creatorcontrib>HYLAND, V. J</creatorcontrib><creatorcontrib>MAY, B. K</creatorcontrib><creatorcontrib>BAWDEN, M. J</creatorcontrib><creatorcontrib>HEALY, H. M</creatorcontrib><creatorcontrib>BORTHWICK, I. A</creatorcontrib><title>5-Aminolevulinate synthase is at 3p21 and thus not the primary defect in X-linked sideroblastic anemia</title><title>American journal of human genetics</title><addtitle>Am J Hum Genet</addtitle><description>The gene for 5-aminolevulinate synthase (ALAS) has been mapped to 3pter-3q13.2 by Southern blot hybridization analysis of a mouse/human hybrid cell panel. In situ hybridization maps the gene to 3p21, distal to the common fragile site at 3p14.2 (FRA3B). The mapping of this gene to an autosome makes it improbable that it is the site of the primary defect in X-linked sideroblastic anemia.</description><subject>5-Aminolevulinate Synthetase - genetics</subject><subject>Anemia, Sideroblastic - genetics</subject><subject>Anemias. Hemoglobinopathies</subject><subject>Biological and medical sciences</subject><subject>Chromosome Mapping</subject><subject>Chromosomes, Human, Pair 3</subject><subject>Cloning, Molecular</subject><subject>Defects</subject><subject>Diseases of red blood cells</subject><subject>Hematologic and hematopoietic diseases</subject><subject>Humans</subject><subject>Medical sciences</subject><subject>Nucleic Acid Hybridization</subject><issn>0002-9297</issn><issn>1537-6605</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1988</creationdate><recordtype>article</recordtype><sourceid>8BJ</sourceid><recordid>eNqFUUtLw0AQDqLUWv0Jwh7EW2D2nVyEUnxBwYuCtzDZbOxqsqnZTaH_3oih6MnTDHwPvvnmKJlTyXWqFMjjZA4ALM1Zrk-TsxDeASjNgM-SGRdUqEzPk1qmy9b5rrG7oXEeoyVh7-MGgyUuEIyEbxkl6CsSN0MgvovjYsm2dy32e1LZ2ppInCev6aj_sBUJrrJ9VzYYojOj0rYOz5OTGptgL6a5SF7ubp9XD-n66f5xtVynWy5ZTGsDGasAsAYqKePAQCuBDAzQUkFVl0Ki4jWAzTRVlCklESTkguXGSsoXyc2P73YoW1sZ62OPTTGlLTp0xV_Eu03x1u0Kqr97E6PB9WTQd5-DDbFoXTC2acY7uiEUOhNA87HE_4hc5ZqznP5LpBKkEBkbiZe_sx9CT78a8asJx2CwqXv0xoUDTWWZzqXgX1QonSA</recordid><startdate>19880901</startdate><enddate>19880901</enddate><creator>SUTHERLAND, G. 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R</au><au>BAKER, E</au><au>CALLEN, D. F</au><au>HYLAND, V. J</au><au>MAY, B. K</au><au>BAWDEN, M. J</au><au>HEALY, H. M</au><au>BORTHWICK, I. A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>5-Aminolevulinate synthase is at 3p21 and thus not the primary defect in X-linked sideroblastic anemia</atitle><jtitle>American journal of human genetics</jtitle><addtitle>Am J Hum Genet</addtitle><date>1988-09-01</date><risdate>1988</risdate><volume>43</volume><issue>3</issue><spage>331</spage><epage>335</epage><pages>331-335</pages><issn>0002-9297</issn><eissn>1537-6605</eissn><coden>AJHGAG</coden><abstract>The gene for 5-aminolevulinate synthase (ALAS) has been mapped to 3pter-3q13.2 by Southern blot hybridization analysis of a mouse/human hybrid cell panel. In situ hybridization maps the gene to 3p21, distal to the common fragile site at 3p14.2 (FRA3B). The mapping of this gene to an autosome makes it improbable that it is the site of the primary defect in X-linked sideroblastic anemia.</abstract><cop>Chicago, IL</cop><pub>University of Chicago Press</pub><pmid>3414687</pmid><tpages>5</tpages></addata></record> |
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source | International Bibliography of the Social Sciences (IBSS); PubMed Central |
subjects | 5-Aminolevulinate Synthetase - genetics Anemia, Sideroblastic - genetics Anemias. Hemoglobinopathies Biological and medical sciences Chromosome Mapping Chromosomes, Human, Pair 3 Cloning, Molecular Defects Diseases of red blood cells Hematologic and hematopoietic diseases Humans Medical sciences Nucleic Acid Hybridization |
title | 5-Aminolevulinate synthase is at 3p21 and thus not the primary defect in X-linked sideroblastic anemia |
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