Publications:

Genetic and clinical specificity of 26 symptomatic carriers for dystrophinopathies at pediatric age.

European Journal Of Human Genetics : Ejhg

Mercier, Sandra S; Toutain, Annick A; Toussaint, Aurélie A; Raynaud, Martine M; de Barace, Claire C; Marcorelles, Pascale P; Pasquier, Laurent L; Blayau, Martine M; Espil, Caroline C; Parent, Philippe P; Journel, Hubert H; Lazaro, Leila L; Andoni Urtizberea, Jon J; Moerman, Alexandre A; Faivre, Laurence L; Eymard, Bruno B; Maincent, Kim K; Gherardi, Romain R; Chaigne, Denys D; Ben Yaou, Rabah R; Leturcq, France F; Chelly, Jamel J; Desguerre, Isabelle I

Publication Date: 2013-08

Variant appearance in text: DMD: 9651C>A; Tyr3217X

PubMed Link: 23299919

Variant Present in the following documents:

• Main text

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