Novel homozygous variants in the TMC1 and CDH23 genes cause autosomal recessive nonsyndromic hearing loss

Abstract Background Hereditary hearing loss (HL) is a heterogeneous and most common sensory neural disorder. At least, 76 genes have been reported in association with autosomal recessive nonsyndromic HL (ARNSHL). Herein, we subjected two patients with bilateral sensorineural HL in two distinct consa...

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Autori principali:	Safoura Zardadi, Ehsan Razmara, Golareh Asgaritarghi, Ehsan Jafarinia, Fatemeh Bitarafan, Sima Rayat, Navid Almadani, Saeid Morovvati, Masoud Garshasbi
Natura:	Artigo
Lingua:	Inglês
Pubblicazione:	Wiley 2020-12-01
Serie:	Molecular Genetics & Genomic Medicine
Soggetti:	cadherin 23 deafness transmembrane channel‐like 1 whole‐exome sequencing
Accesso online:	https://doi.org/10.1002/mgg3.1550
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