Associated Papers
The c.644 G > A p.(Trp215*) founder variant in the CLIC5 gene causes progressive autosomal recessive deafness 103 (DFNB103) in Eastern Siberia.
Pshennikova VG et al.
Journal of Human Genetics, 2026
Features of autosomal recessive non-syndromic hearing impairment: a review to serve as a reference.
Oonk AM et al.
Clinical Otolaryngology : Official Journal of Ent-uk ; Official Journal of Netherlands Society for Oto-rhino-laryngology & Cervico-facial Surgery, 2016
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