Novel ACTG1 mutation causing autosomal dominant non-syndromic hearing impairment in a Chinese family
ISSN号:1673-8527
期刊名称:《遗传学报:英文版》
时间:0
分类:Q754[生物学—分子生物学]
作者机构:[1]Key Laboratory of Molecular Biophysics of Ministry of Education, Center for Human Genome Research, College of Life Science and Technology, Huazhong University of Science and Technology, Wuhan 430074, China, [2]The Fourth People's Hospital ofYancheng, Yancheng 224000, Jiangsu, China
相关基金:We thank the patients and families for their enthusiastic participation and support. This study was supported by the National Natural Science Foundation of China (No. 30670736 and 30500168), and the Department of Science and Technology of Jiangsu Province (No. BS2006533).