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International Journal of Pediatric Otorhinolaryngology|October 2, 2017
Novel pathogenic variants underlie SLC26A4-related hearing loss in a multiethnic cohortFiliz Basak Cengiz, Rasim Yilmazer, Levent Olgun, et al.Human Genomics|April 3, 2024
The genetic basis of early-onset hereditary ataxia in Iran: results of a national registry of a heterogeneous populationNejat Mahdieh, Morteza Heidari, Zahra Rezaei, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 31, 2015
Comprehensive analysis via exome sequencing uncovers genetic etiology in autosomal recessive nonsyndromic deafness in a large multiethnic cohortGuney Bademci, Joseph Foster, Nejat Mahdieh, et al.Neurogenetics|August 19, 2023
High genetic heterogeneity of leukodystrophies in Iranian children: the first report of Iranian Leukodystrophy RegistryMahmoudreza Ashrafi, Reyhaneh Kameli, Sareh Hosseinpour, et al.Pageof 10