The p.(Pro170Leu) variant in NOG impairs noggin secretion and causes autosomal dominant congenital conductive hearing loss due to stapes ankylosis

Yilai ShuLijun WangXiaoting ChengChayada TangshewinsirikulWeili ShiYasheng YuanZhiqiang YanHuawei LiJun ShenBing ChenWeiguo ZouSchool of Life Sciences Fudan UniversityZhengzhou UniversityBrigham and Women's HospitalFaculty of Medicine, Ramathibodi Hospital, Mahidol UniversityFudan UniversityHarvard Medical School Center for Hereditary DeafnessShanghai Institute for Biological Sciences Chinese Academy of Sciences2020-01-272020-01-272019-09-20Journal of Genetics and Genomics. Vol.46, No.9 (2019), 445-44918735533167385272-s2.0-85075078839https://repository.li.mahidol.ac.th/handle/20.500.14594/50079Mahidol UniversityBiochemistry, Genetics and Molecular BiologyThe p.(Pro170Leu) variant in NOG impairs noggin secretion and causes autosomal dominant congenital conductive hearing loss due to stapes ankylosisLetterSCOPUS10.1016/j.jgg.2019.09.003