Haplotype Analysis Reveals a Possible Founder Effect of RET Mutation R114H for Hirschsprung's Disease in the Chinese Population-Reference-Cited by-同舟云学术

Haplotype Analysis Reveals a Possible Founder Effect of RET Mutation R114H for Hirschsprung's Disease in the Chinese Population

Published:2010-06-02 Issue:6 Volume:5 Page:e10918
ISSN:1932-6203
Container-title:PLoS ONE
language:en
Short-container-title:PLoS ONE

Author:

Cornes Belinda K.,Tang Clara S.,Leon Thomas Y. Y.,Hui Kenneth J. W. S.,So Man-Ting,Miao Xiaoping,Cherny Stacey S.,Sham Pak C.,Tam Paul K. H.,Garcia-Barcelo Maria-Merce

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference22 articles.

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2. Hirschsprung Disease.;A Chakravarti,2001

3. A gene for Hirschsprung disease maps to the proximal long arm of chromosome 10.;S Lyonnet;Nat Genet,1993

4. RET-deficient mice: an animal model for Hirschsprung's disease and renal agenesis.;A Schuchardt;J Intern Med,1995

5. A common sex-dependent mutation in a RET enhancer underlies Hirschsprung disease risk.;ES Emison;Nature,2005

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