DMD c.9134T>C ;(p.F3045S)

Variant ID: X-31366702-A-G

NM_004006.2(DMD):c.9134T>C;(p.F3045S)

This variant was identified in 1 publication

View GRCh38 version.




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: Phe3045Ser
PubMed Link: 23299919
Variant Present in the following documents:
  • Main text
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