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Mutations in BCAP31 cause a severe X-linked phenotype with deafness, dystonia, and central hypomyelination and disorganize the Golgi apparatus
scientific article published on September 2013
Author/s
author: Jean-Christophe Roux, Jean-Pierre Desvignes, Nicolas Levy, Laurent Villard, Mark Lathrop
Work details
Publication date
September 1, 2013
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Language
English
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