Mutations in BCAP31 Cause a Severe X-Linked Phenotype with Deafness, Dystonia, and Central Hypomyelination and Disorganize the Golgi Apparatus
Titel:
Mutations in BCAP31 Cause a Severe X-Linked Phenotype with Deafness, Dystonia, and Central Hypomyelination and Disorganize the Golgi Apparatus
Auteur:
Cacciagli, Pierre Sutera-Sardo, Julie Borges-Correia, Ana Roux, Jean-Christophe Dorboz, Imen Desvignes, Jean-Pierre Badens, Catherine Delepine, Marc Lathrop, Mark Cau, Pierre Lévy, Nicolas Girard, Nadine Sarda, Pierre Boespflug-Tanguy, Odile Villard, Laurent