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Article

Potential Association of INMT Nonsynonymous Variant (His46Pro) with Hirschsprung's Disease.

Neonatology - 1 Jan 2015

Kim Jason Yongha, Seo Jeong-Meen, Kim Dae-Yeon, Oh Jung-Tak, Park Kwi-Won, Kim Hyun-Young, Jung Kyuwhan, Park Byung Lae, Kim Jeong-Hyun, Shin Hyoung Doo

Abstract excerpt

BACKGROUND: Hirschsprung's disease (HSCR) is a congenital disorder which is characterized by the lack of ganglion cells in part of or the entire colon, resulting in intestinal obstruction and other related symptoms. Recently, our group has conducted a genome-wide association study in Korean HSCR cases and controls to identify novel markers in other genes. OBJECTIVES: The present research aimed to further study...

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Source

Identifiers

PMID: 26183064
DOI: 10.1159/000435874

Genes

INMT

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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