A novel mutation in the Espin gene causes autosomal recessive nonsyndromic hearing loss but no apparent vestibular dysfunction in a Moroccan family.
作者信息
Boulouiz Redouane, Li Yun, Soualhine Hafid, Abidi Omar, Chafik Abdelaziz, Nürnberg Gudrun, Becker Christian, Nürnberg Peter, Kubisch Christian, Wollnik Bernd, Barakat Abdelhamid
机构信息
Department of Genetics, Institut Pasteur du Maroc, Casablanca, Morocco.
出版信息
Am J Med Genet A. 2008 Dec 1;146A(23):3086-9. doi: 10.1002/ajmg.a.32525.
PMID:18973245
Abstract
摘要
Zotero 插件