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

Publication date: Available online 27 September 2019Source: Journal of Genetics and GenomicsAuthor(s): Yilai Shu, Lijun Wang, Xiaoting Cheng, Chayada Tangshewinsirikul, Weili Shi, Yasheng Yuan, Zhiqiang Yan, Huawei Li, Jun Shen, Bing Chen, Weiguo Zou

Source: Journal of Genetics and Genomics - September 28, 2019 Category: Genetics & Stem Cells Source Type: research