Effects of RET and NRG1 polymorphisms in Indonesian patients with Hirschsprung disease

BACKGROUND: Hirschsprung disease (HSCR) is a neurocristopathy characterized by absence of intramural ganglion cells along variable lengths of the gastrointestinal tract in neonates. Three polymorphisms, rs2435357, within a conserved transcriptional enhancer of RET, and, rs7835688 and rs16879552, wit...

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Bibliografiska uppgifter
I publikationen:J Pediatr Surg
Huvudupphovsmän: Gunadi, Kapoor, Ashish, Ling, Albee Yun, Rochadi, Makhmudi, Akhmad, Herini, Elisabeth Siti, Sosa, Maria X., Chatterjee, Sumantra, Chakravarti, Aravinda
Materialtyp: Artigo
Språk:Inglês
Publicerad: 2014
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Article
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC4258000/
https://ncbi.nlm.nih.gov/pubmed/25475805
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jpedsurg.2014.04.011
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