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Autor:
Doo-Yi Oh, Heon Yung Gee, Sang-Yeon Lee, Ami Kim, Jieun An, Bong Jik Kim, Na-Young Yi, Jin Hee Han, Min Young Kim, Seungmin Lee, Chung Lee, Nahyun Kim, Young Ik Koh, Eunku Kim, Hyun Been Choi, Hyun Sung Cho, Woong-Yang Park, Byung Yoon Choi, Tong Mook Kang, Mina Park, Il Soon Choi, Nayoung K.D. Kim
Publikováno v:
Experimental & Molecular Medicine
Loss-of-function variant in the gene encoding the KCNQ4 potassium channel causes autosomal dominant nonsyndromic hearing loss (DFNA2), and no effective pharmacotherapeutics have been developed to reverse channel activity impairment. Phosphatidylinosi