2020. May

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.

Ann Lab Med. 2020

Song JS, Bahloul A, Petit C, Kim SJ, Moon IJ, Lee J, Ki CS.