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Literature DB >> 16040858

Novel RET mutation produces a truncated RET receptor lacking the intracellular signaling domain in a 3-generation family with Hirschsprung disease.

Abstract

Entities: Disease Gene

Source DB: PubMed Journal: Clin Chem ISSN： 0009-9147 Impact factor: 8.327

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Authors: Jiang Zhu; Maria-Mercedes Garcia-Barcelo; Paul Kwong Hang Tam; Vincent Chi Hang Lui
Journal: PLoS One Date: 2011-06-03 Impact factor: 3.240

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