Atie Kashef

A novel mutation of the USH2C (GPR98) gene in an Iranian family with Usher syndrome type II

K. Kahrizi, H. Najmabadi, Niloofar Bazazzadegan, 2014, Journal of Genetics.

Finding mutation within non-coding region of GJB2 reveals its importance in genetic testing of hearing loss in Iranian population.

K. Kahrizi, H. Najmabadi, F. Mojahedi, 2015, International journal of pediatric otorhinolaryngology.

The spectrum of GJB2 mutations in the Iranian population with non-syndromic hearing loss--a twelve year study.

K. Kahrizi, H. Najmabadi, F. Mojahedi, 2012, International journal of pediatric otorhinolaryngology.

Further delineation of the phenotype caused by a novel large homozygous deletion of GRID2 gene in an adult patient

M. Fardaei, R. Kariminejad, Maryam Taghdiri, 2019, Clinical case reports.

Identification of a novel deletion within ALDH3A2 gene in an Iranian Family with Sjögren–Larsson Syndrome

M. Miryounesi, M. Fardaei, Maryam Taghdiri, 2017, Clinical case reports.

A novel mutation of the USH2C (GPR98) gene in an Iranian family with Usher syndrome type II

K. Kahrizi, H. Najmabadi, Niloofar Bazazzadegan, 2014, Journal of Genetics.

Further delineation of the phenotype caused by a novel large homozygous deletion of GRID2 gene in an adult patient

M. Fardaei, R. Kariminejad, Maryam Taghdiri, 2019, Clinical case reports.