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Genetic and clinical specificity of 26 symptomatic carriers for dystrophinopathies at pediatric age.
Mercier, Sandra; Toutain, Annick; Toussaint, Aurélie; Raynaud, Martine; de Barace, Claire; Marcorelles, Pascale; Pasquier, Laurent; Blayau, Martine; Espil, Caroline; Parent, Philippe; Journel, Hubert; Lazaro, Leila; Andoni Urtizberea, Jon; Moerman, Alexandre; Faivre, Laurence; Eymard, Bruno; Maincent, Kim; Gherardi, Romain; Chaigne, Denys; Ben Yaou, Rabah; Leturcq, France; Chelly, Jamel; Desguerre, Isabelle.
Affiliation
  • Mercier S; Department of Medical Genetics, CHU Nantes, France.
Eur J Hum Genet ; 21(8): 855-63, 2013 Aug.
Article in En | MEDLINE | ID: mdl-23299919
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Dystrophin / Muscular Dystrophy, Duchenne / Heterozygote / Muscles Type of study: Diagnostic_studies Limits: Adolescent / Adult / Aged / Child / Child, preschool / Female / Humans / Middle aged Country/Region as subject: Europa Language: En Journal: Eur J Hum Genet Journal subject: GENETICA MEDICA Year: 2013 Document type: Article Affiliation country: France Country of publication: United kingdom
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Dystrophin / Muscular Dystrophy, Duchenne / Heterozygote / Muscles Type of study: Diagnostic_studies Limits: Adolescent / Adult / Aged / Child / Child, preschool / Female / Humans / Middle aged Country/Region as subject: Europa Language: En Journal: Eur J Hum Genet Journal subject: GENETICA MEDICA Year: 2013 Document type: Article Affiliation country: France Country of publication: United kingdom