Whole exome sequencing revealed biallelic IFT122 mutations in a family with CED1 and recurrent pregnancy loss.
作者信息
Tsurusaki Y, Yonezawa R, Furuya M, Nishimura G, Pooh R K, Nakashima M, Saitsu H, Miyake N, Saito S, Matsumoto N
机构信息
Department of Human Genetics, Yokohama City Graduate School of Medicine, Yokohama, Japan.
出版信息
Clin Genet. 2014 Jun;85(6):592-4. doi: 10.1111/cge.12215. Epub 2013 Jul 5.
PMID:23826986
Abstract
摘要
Zotero 插件