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Article

Investigation of MYO15A and MYO7A Mutations in Iranian Patients with Nonsyndromic Hearing Loss.

Fetal and pediatric pathology - 1 Apr 2021

Farjami Mahsa, Fathi Mozhgan, Ghasemi Mohammad Mehdi, Rajati Mohsen, Eslahi Atieh, Alimardani Malihe, Mojarrad Majid

Abstract excerpt

BACKGROUND: Hearing loss (HL) is the most common sensory disorder in humans, which affects individuals in both inherited and acquired forms. MYO15A and MYO7A gene mutations have a significant role in the development of deafness. In this study, we assessed the prevalence of MYO15A and MYO7A mutations in one hundred non-relative deaf Iranians. Materials and methods: The existence of MYO15A and MYO7A mutations were...

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Identifiers

PMID: 31997689
DOI: 10.1080/15513815.2019.1686790

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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