Telomere shortening by mutations in the RTEL1 helicase cause severe form of dyskeratosis congenita, Hoyerall-Hreidarsson syndrome.
作者信息
Lee J W
机构信息
Department of Medical Genetics, The Canadian Pharmacogenomic Network for Drug Safety (CPNDS), Center for Molecular Medicine and Therapeutics, University of British Columbia, 950 West 28th Avenue, Vancouver, British Columbia, V5Z4H4, Canada.
出版信息
Clin Genet. 2013 Sep;84(3):210. doi: 10.1111/cge.12175. Epub 2013 May 27.
PMID:23621889
Abstract
摘要
Zotero 插件