A Novel Heterozygous Missense Variant (c.667G>T;p.Gly223Cys) in USH1C That Interferes With Cadherin-Related 23 and Harmonin Interaction Causes Autosomal Dominant Nonsyndromic Hearing Loss
Ju Sun Song , M.D., Amel Bahloul
, Ph.D., Christine Petit
, M.D., Ph.D., Sang Jin Kim
, M.D., Ph.D., Il Joon Moon
, M.D., Ph.D., Jinhyuk Lee
, Ph.D., and Change-Seok Ki
, M.D., Ph.D.
https://doi.org/10.3343/alm.2020.40.3.224