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Article

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

PloS one - 1 Jan 2017

Bakhchane Amina, Charif Majida, Bousfiha Amale, Boulouiz Redouane, Nahili Halima, Rouba Hassan, Charoute Hicham, Lenaers Guy, Barakat Abdelhamid

Abstract excerpt

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 non syndromic hearing loss that identified two families with compound heterozygous MYO7A mutations. Five mutations...

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PMID: 28472130
DOI: 10.1371/journal.pone.0176516
PMCID: PMC5417485

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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