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Articles that cite the referenced work, matched by title from the Scopus database.

4 resultsUpdated October 21, 2026

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1

Whole-Exome Sequencing Identifies a Recurrent Small In-Frame Deletion in MYO15A Causing Autosomal Recessive Nonsyndromic Hearing Loss in 3 Iranian Pedigrees

Lab Medicine

1 March 2022

Nasrniya S.

2

Identification of a novel frameshift mutation in the tecta gene in an iranian family with autosomal nonsyndromic hearing loss

Acta Medica Iranica

2021

Mohammadi-Asl J.

Open Access

3

Novel mutations in MYTH4-FERM domains of myosin 15 are associated with autosomal recessive nonsyndromic hearing loss

International Journal of Pediatric Otorhinolaryngology

February 2019

Mehregan H.

4

Next-generation sequencing identifies three novel missense variants in ILDR1 and MYO6 genes in an Iranian family with hearing loss with review of the literature

International Journal of Pediatric Otorhinolaryngology

December 2017

Talebi F.