RET variants and haplotype analysis in a cohort of Czech patients with Hirschsprung disease.

RET variants and haplotype analysis in a cohort of Czech patients with Hirschsprung disease.

Hirschsprung disease (HSCR) is a congenital aganglionosis of myenteric and submucosal plexuses in variable length of the intestine. This study investigated the influence and a possible modifying function of RET proto-oncogene's single nucleotide polymorphisms (SNPs) and haplotypes in the develo...

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Bibliographic Details
Main Authors: Eliska Vaclavikova, Sarka Dvorakova, Richard Skaba, Lucie Pos, Vlasta Sykorova, Tereza Halkova, Josef Vcelak, Bela Bendlova
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4045806?pdf=render

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