A Genome-Wide Association Study Identifies Potential Susceptibility Loci for Hirschsprung Disease

Hirschsprung disease (HSCR) is a congenital and heterogeneous disorder characterized by the absence of intramural nervous plexuses along variable lengths of the hindgut. Although RET is a well-established risk factor, a recent genome-wide association study (GWAS) of HSCR has identified NRG1 as an ad...

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Detalles Bibliográficos
Autores principales: Kim, Jeong-Hyun, Cheong, Hyun Sub, Sul, Jae Hoon, Seo, Jeong-Meen, Kim, Dae-Yeon, Oh, Jung-Tak, Park, Kwi-Won, Kim, Hyun-Young, Jung, Soo-Min, Jung, Kyuwhan, Cho, Min Jeng, Bae, Joon Seol, Shin, Hyoung Doo
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/PMC4195606/
https://www.ncbi.nlm.nih.gov/pubmed/25310821
http://dx.doi.org/10.1371/journal.pone.0110292

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4195606/
https://www.ncbi.nlm.nih.gov/pubmed/25310821
http://dx.doi.org/10.1371/journal.pone.0110292

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