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. 2013 Jul 18;21(8):892. doi: 10.1038/ejhg.2013.74

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

Sandra Mercier 1,2, Annick Toutain 3, Aurélie Toussaint 2, Martine Raynaud 3, Claire de Barace 4, Pascale Marcorelles 5, Laurent Pasquier 6, Martine Blayau 7, Isabelle Pénisson-Besnier 8, Norma Romero 9, Caroline Espil 10, Philippe Parent 11, Hubert Journel 12, Leila Lazaro 13, Jon Andoni Urtizberea 14, Alexandre Moerman 15, Laurence Faivre 16, Bruno Eymard 17, Kim Maincent 18, Romain Gherardi 19, Denys Chaigne 20, Rabah Ben Yaou 2, France Leturcq 2, Jamel Chelly 2, Isabelle Desguerre 2,21
PMCID: PMC3722685

Correction to: European Journal of Human Genetics (2013) advance online publication, 9 January 2013; doi:10.1038/ejhg.2012.269

Since the publication of this article, the authors asked for the additional affiliation of two authors, Isabelle Pénisson-Besnier and Norma Romero. These have now been added and the amended article appears in this issue. The HTML and online PDF versions have also been amended and now carry the additional affiliations.

Articles from European Journal of Human Genetics are provided here courtesy of Nature Publishing Group

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