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Select item 46622671.

A Novel de novo Mutation in CEACAM16 Associated with Postlingual Hearing Impairment

Michaela A.H. Hofrichter, Indrajit Nanda, Jens Gräf, Jörg Schröder, Wafaa Shehata-Dieler, Barbara Vona, Thomas Haaf

Mol Syndromol. 2015 Oct; 6(4): 156–163. Published online 2015 Sep 3. doi: 10.1159/000439576

PMCID:: PMC4662267

Article PDF–265K

Select item 43750192.

Exome Sequencing Identifies a Novel CEACAM16 Mutation Associated with Autosomal Dominant Nonsyndromic Hearing Loss DFNA4B in a Chinese Family

Honghan Wang, Xinwei Wang, Chufeng He, Haibo Li, Jie Qing, Mhamed Grati, Zhengmao Hu, Jiada Li, Yiqiao Hu, Kun Xia, Lingyun Mei, Xingwei Wang, Jianjun Yu, Hongsheng Chen, Lu Jiang, Yalan Liu, Meichao Men, Hailin Zhang, Liping Guan, Jingjing Xiao, Jianguo Zhang, Xuezhong Liu, Yong Feng

J Hum Genet. Author manuscript; available in PMC 2015 Sep 1.

Published in final edited form as: J Hum Genet. 2015 Mar; 60(3): 119–126. Published online 2015 Jan 15. doi: 10.1038/jhg.2014.114