Items where Author is "Asgharzade, S."

(2018) A novel missense mutation in GIPC3 causes sensorineural hearing loss in an Iranian family revealed by targeted next-generation sequencing. International Journal of Pediatric Otorhinolaryngology. pp. 8-11. ISSN 0165-5876

(2017) Screening of Myo7A Mutations in Iranian Patients with Autosomal Recessive Hearing Loss from West of Iran. Iranian Journal of Public Health. pp. 76-82. ISSN 2251-6085

(2017) A novel TECTA mutation causes ARNSHL. International Journal of Pediatric Otorhinolaryngology. pp. 88-93. ISSN 0165-5876

(2016) Mutation in Second Exon of Myo15a Gene Cause of Nonsyndromic Hearing Loss and Its Association in the Arab Population in Iran. Genetika-Belgrade. pp. 587-596. ISSN 0534-0012