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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Detalhes bibliográficos
Main Authors: Vaclavikova, Eliska, Dvorakova, Sarka, Skaba, Richard, Pos, Lucie, Sykorova, Vlasta, Halkova, Tereza, Vcelak, Josef, Bendlova, Bela
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2014
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4045806/
https://ncbi.nlm.nih.gov/pubmed/24897126
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0098957
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