Associated Papers
Molecular diagnosis of SLC26A4-related hereditary hearing loss in a group of patients from two provinces of Iran.
Koohiyan M et al.
Intractable & Rare Diseases Research, 2021
An update of common autosomal recessive non-syndromic hearing loss genes in Iranian population.
Ghasemnejad T et al.
International Journal of Pediatric Otorhinolaryngology, 2017
The role and spectrum of SLC26A4 mutations in Iranian patients with autosomal recessive hereditary deafness.
Yazdanpanahi N et al.
International Journal of Audiology, 2015
Compound Heterozygosity for Two Novel SLC26A4 Mutations in a Large Iranian Pedigree with Pendred Syndrome.
Yazdanpanahi N et al.
Clinical and Experimental Otorhinolaryngology, 2013
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