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Article

Homozygous mutations in PJVK and MYO15A genes associated with non-syndromic hearing loss in Moroccan families.

International journal of pediatric otorhinolaryngology - 1 Oct 2017

Salime Sara, Charif Majida, Bousfiha Amale, Elrharchi Soukaina, Bakhchane Amina, Charoute Hicham, Kabine Mostafa, Snoussi Khalid, Lenaers Guy, Barakat Abdelhamid

Abstract excerpt

OBJECTIVES: Autosomal recessive non-syndromic hearing loss is a heterogeneous disorder and the most prevalent human genetic sensorineural defect. In this study, we investigated the geneticcause of sensorineural hearing loss in Moroccan patients and presented the importance of whole exome sequencing (WES) to identify candidate genes in two Moroccan families with profound deafness. METHODS: After excluding...

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Source

Identifiers

PMID: 28964305
DOI: 10.1016/j.ijporl.2017.07.024

Genes

PJVK

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

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