Two large French pedigrees with non syndromic sensorineural deafness and the mitochondrial DNA T7511C mutation: evidence for a modulatory factor
Élise Chapiro(Sorbonne Université), Sandrine Marlin(Hôpital Necker-Enfants Malades), Dominique Weil(Boys Town), Christine Petit(Inserm), Françoise Denoyelle(Hôpital Necker-Enfants Malades), Claude Jardel(Sorbonne Université), D. Bouccara(Centre National de la Recherche Scientifique), Éréa-Noël Garabédian(Inserm), Delphine Feldmann(Hôpital Armand-Trousseau), Marie‐Madeleine Eliot, Rémy Couderc(Sorbonne Université), Damien Sternberg(Children's Hospital of Philadelphia)
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