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Human Genetics|January 26, 2021
A biallelic variant in CLRN2 causes non-syndromic hearing loss in humansBarbara Vona, Neda Mazaheri, Sheng-Jia Lin, et al.
EMBO Molecular Medicine|August 27, 2019
Clarin-2 is essential for hearing by maintaining stereocilia integrity and functionLucy A Dunbar, Pranav Patni, Carlos Aguilar, et al.
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