Novel compound heterozygous MYO7A mutations in Moroccan families with autosomal recessive non-syndromic hearing loss

The MYO7A gene encodes a protein belonging to the unconventional myosin super family. Mutations within MYO7A can lead to either non syndromic hearing loss or to the Usher syndrome type 1B (USH1B). Here, we report the results of genetic analyses performed on Moroccan families with autosomal recessive...

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Detalles Bibliográficos
Autores principales: Bakhchane, Amina, Charif, Majida, Bousfiha, Amale, Boulouiz, Redouane, Nahili, Halima, Rouba, Hassan, Charoute, Hicham, Lenaers, Guy, Barakat, Abdelhamid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5417485/
https://www.ncbi.nlm.nih.gov/pubmed/28472130
http://dx.doi.org/10.1371/journal.pone.0176516

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5417485/
https://www.ncbi.nlm.nih.gov/pubmed/28472130
http://dx.doi.org/10.1371/journal.pone.0176516

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