Mohammad Amin Tabatabaiefar

Molecular diagnostics for congenital hearing loss including 15 deafness genes using a next generation sequencing platform

Sarah De Keulenaer, Jan Hellemans, Steve Lefever et al. · BMC Medical Genomics · 2012 · 57 citations · Full text

A novel variant of SLC26A4 and first report of the c.716T>A variant in Iranian pedigrees with non-syndromic sensorineural hearing loss

Fatemeh Azadegan‐Dehkordi, Reza Ahmadi, Tayyeb Bahrami et al. · American Journal of Otolaryngology · 2018 · 16 citations

Novel Variant, Genetics, Audiology +9

A Novel Pathogenic Variant in the CABP2 Gene Causes Severe Nonsyndromic Hearing Loss in a Consanguineous Iranian Family

Mahbobeh Koohiyan, Mohammad Reza Noori–Daloii, Morteza Hashemzadeh‐Chaleshtori et al. · Audiology and Neurotology · 2019 · 16 citations

Compound Heterozygosity for Two Novel<i>SLC26A4</i>Mutations in a Large Iranian Pedigree with Pendred Syndrome

Nasrin Yazdanpanahi, Mohammad Amin Tabatabaiefar, Effat Farrokhi et al. · Clinical and Experimental Otorhinolaryngology · 2013 · 15 citations · Full text

Whole exome sequencing identifies novel compound heterozygous pathogenic variants in the MYO15A gene leading to autosomal recessive non-syndromic hearing loss

Akram Sarmadi, Samane Nasrniya, Sina Narrei et al. · Molecular Biology Reports · 2020 · 12 citations

Mendelian Disorder, Genetic Disorder, Genetics +13