Novel RET mutation produces a truncated RET receptor lacking the intracellular signaling domain in a 3-generation family with Hirschsprung disease.
作者信息
Lui Vincent C H, Leon Thomas Y Y, Garcia-Barceló Maria-Mercedes, Ganster Raymond W, Chen Benedict L S, Hutson John M, Tam Paul K H
机构信息
Department of Surgery and Genome Research Centre, The University of Hong Kong Pokfulam, Hong Kong SAR, China.
出版信息
Clin Chem. 2005 Aug;51(8):1552-4. doi: 10.1373/clinchem.2005.051904.
PMID:16040858
Abstract
摘要
Zotero 插件