Gènètique : Des variants récessifs du gène COL25A1 comme nouvelle cause d’arthrogrypose multiple congénitale avec dysinnervation des nerfs crâniens oculaires
{"title":"Gènètique : Des variants récessifs du gène COL25A1 comme nouvelle cause d’arthrogrypose multiple congénitale avec dysinnervation des nerfs crâniens oculaires","authors":"Valérie Allamand","doi":"10.1051/myolog/202225011","DOIUrl":null,"url":null,"abstract":"","PeriodicalId":181474,"journal":{"name":"Les Cahiers de Myologie","volume":"24 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2022-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Les Cahiers de Myologie","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1051/myolog/202225011","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
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