A recurrent p. A353V mutation in DKC1 responsible for different phenotypes of dyskeratosis congenita in a Chinese family.
作者信息
Lai W, Deng W P, Liu X, Chen H M, Dai Sh X
出版信息
J Dermatol Sci. 2011 Aug;63(2):122-4. doi: 10.1016/j.jdermsci.2011.04.009. Epub 2011 Apr 28.
Abstract
摘要
Zotero 插件