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3 resultsUpdated October 23, 2026

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1

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 103 (2017)

Farah Talebi; Farideh Ghanbari Mardasi; Javad Mohammadi Asl; Masoomeh Sayahi

2

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

International Journal of Pediatric Otorhinolaryngology 117 (2018)

Hoda Mehregan; Marzieh Mohseni; Khadijeh Jalalvand; Sanaz Arzhangi; Nooshin Nikzat; Sussan Banihashemi; Kimia Kahrizi; Hossein Najmabadi

3

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

Laboratory Medicine 53(2) (2021)

Samane Nasrniya; Paniz Miar; Sina Narrei; Mahsa Sepehrnejad; Mohammad Hossein Nilforoush; Hamidreza Abtahi; Mohammad Amin Tabatabaiefar