Screening of the CAPN3 gene in patients with possible LGMD2A
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Veröffentlicht in: | Clinical genetics 2006-05, Vol.69 (5), p.444-449 |
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creator | Krahn, Martin Bernard, Rafaëlle Pécheux, Christophe Hammouda, El Hadi Eymard, Bruno Munain, Adolfo Lopez de Cobo, Anna Maria Romero, Norma Urtizberea, Andoni Leturcq, France Lévy, Nicolas |
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doi_str_mv | 10.1111/j.1399-0004.2006.00603.x |
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Genetic counseling</topic><topic>Genetic Testing</topic><topic>Humans</topic><topic>Male</topic><topic>Medical genetics</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Muscle Proteins - genetics</topic><topic>Muscular Dystrophies, Limb-Girdle - diagnosis</topic><topic>Muscular Dystrophies, Limb-Girdle - genetics</topic><topic>Mutation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Krahn, Martin</creatorcontrib><creatorcontrib>Bernard, Rafaëlle</creatorcontrib><creatorcontrib>Pécheux, Christophe</creatorcontrib><creatorcontrib>Hammouda, El Hadi</creatorcontrib><creatorcontrib>Eymard, Bruno</creatorcontrib><creatorcontrib>Munain, Adolfo Lopez de</creatorcontrib><creatorcontrib>Cobo, Anna Maria</creatorcontrib><creatorcontrib>Romero, Norma</creatorcontrib><creatorcontrib>Urtizberea, Andoni</creatorcontrib><creatorcontrib>Leturcq, France</creatorcontrib><creatorcontrib>Lévy, Nicolas</creatorcontrib><creatorcontrib>Calpain Study Group of the French LGMD Network</creatorcontrib><creatorcontrib>The Calpain study group of the French LGMD network</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Clinical genetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Krahn, Martin</au><au>Bernard, Rafaëlle</au><au>Pécheux, Christophe</au><au>Hammouda, El Hadi</au><au>Eymard, Bruno</au><au>Munain, Adolfo Lopez de</au><au>Cobo, Anna Maria</au><au>Romero, Norma</au><au>Urtizberea, Andoni</au><au>Leturcq, France</au><au>Lévy, Nicolas</au><aucorp>Calpain Study Group of the French LGMD Network</aucorp><aucorp>The Calpain study group of the French LGMD network</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Screening of the CAPN3 gene in patients with possible LGMD2A</atitle><jtitle>Clinical genetics</jtitle><addtitle>Clin Genet</addtitle><date>2006-05</date><risdate>2006</risdate><volume>69</volume><issue>5</issue><spage>444</spage><epage>449</epage><pages>444-449</pages><issn>0009-9163</issn><eissn>1399-0004</eissn><coden>CLGNAY</coden><cop>Oxford, UK; Malden, USA</cop><pub>Blackwell Publishing Ltd</pub><pmid>16650086</pmid><doi>10.1111/j.1399-0004.2006.00603.x</doi><tpages>6</tpages></addata></record> |
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subjects | Adolescent Adult Aged Biological and medical sciences Calpain - genetics Child DNA Mutational Analysis Female General aspects. Genetic counseling Genetic Testing Humans Male Medical genetics Medical sciences Middle Aged Muscle Proteins - genetics Muscular Dystrophies, Limb-Girdle - diagnosis Muscular Dystrophies, Limb-Girdle - genetics Mutation |
title | Screening of the CAPN3 gene in patients with possible LGMD2A |
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