Hyaluronan Synthase 1: A Novel Candidate Gene Associated With Late-Onset Non-syndromic Hereditary Hearing Loss
Clinical and Experimental Otorhinolaryngology. 2022;15(3):220-229 
Gene mapping of non-syndromic hereditary hearing loss
International Journal of Pediatric Otorhinolaryngology. 1997;39(3):246-247
Late-onset hearing loss in a mouse model of DFN3 non-syndromic deafness: morphologic and immunohistochemical analyses
Hearing Research. 2002;166(1-2):150-158
A novel splice site mutation in DFNA5 causes late-onset progressive non-syndromic hearing loss in a Chinese family
International Journal of Pediatric Otorhinolaryngology. 2014;78(8):1265-1268
Hereditary Non-Syndromic Sensorineural Hearing Loss
The Journal of Molecular Diagnostics. 2004;6(4):275-284
Novel mutations in the pejvakin gene are associated with autosomal recessive non-syndromic hearing loss in Iranian families
Clinical Genetics. 2007;72(3):261-263
A novel dominant missense mutation - D179N - in theGJB2gene (Connexin 26) associated with non-syndromic hearing loss
Clinical Genetics. 2003;63(6):516-521
Variants in CDH23 Cause Broad Spectrum of Hearing Loss: From Non-Syndromic to Syndromic Hearing Loss as Well as From Congenital to Age-Related Hearing Loss
. 2021;
A novel mutation in the TMC1 gene causes non-syndromic hearing loss in a Moroccan family.
Gene. 2015;574(1):28-33
Whole Exome Sequencing of Six Chinese Families with Hereditary Non-syndromic Hearing Loss
. 2021;