An update on autosomal recessive hearing loss and loci involved in it
Author:
Publisher
Medknow
Subject
Otorhinolaryngology
Reference107 articles.
1. Azadegan-Dehkordi F, Ahmadi R, Koohiyan M, Hashemzadeh-Chaleshtori M. Update of spectrum c. 35delG and c.-23+1G>A mutations on the GJB2 gene in individuals with autosomal recessive nonsyndromic hearing loss. Ann Hum Genet 2018;83:1-10.
2. Compound heterozygosity for two novel SLC26A4 mutations in a large Iranian pedigree with Pendred syndrome;Yazdanpanahi;Clin Exp Otorhinolaryngol,2013
3. Mutations in GJB2 as major causes of autosomal recessive non-syndromic hearing loss: First report of c.299-300delAT mutation in Kurdish population of Iran;Azadegan-Dehkordi;Korean J Audiol,2019
4. Large-scale screening of mitochondrial DNA mutations among Iranian patients with prelingual nonsyndromic hearing impairment;Montazer;Genet Test Mol Biomarkers,2012
5. A novel variant of SLC26A4 and first report of the c.716T>A variant in Iranian pedigrees with non-syndromic sensorineural hearing loss;Azadegan-Dehkordi;Am J Otolaryngol,2018
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