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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Detalles Bibliográficos
Autores principales: Vaclavikova, Eliska, Dvorakova, Sarka, Skaba, Richard, Pos, Lucie, Sykorova, Vlasta, Halkova, Tereza, Vcelak, Josef, Bendlova, Bela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4045806/
https://www.ncbi.nlm.nih.gov/pubmed/24897126
http://dx.doi.org/10.1371/journal.pone.0098957

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4045806/
https://www.ncbi.nlm.nih.gov/pubmed/24897126
http://dx.doi.org/10.1371/journal.pone.0098957

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