Analysis of the RET, GDNF, EDN3, and EDNRB genes in patients with intestinal neuronal dysplasia and Hirschsprung disease

BACKGROUND—Hirschsprung disease (HSCR) is a frequent congenital disorder with an incidence of 1 in 5000 live births, characterised by the absence of parasympathetic intramural ganglion cells in the hindgut resulting in intestinal obstruction in neonates and severe constipation in infants and adults....

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Autori principali: Gath, R, Goessling, A, Keller, K, Koletzko, S, Coerdt, W, Muntefering, H, Wirth, S, Hofstra, R, Mulligan, L, Eng, C, von Deimling, A
Natura: Artigo
Lingua:Inglês
Pubblicazione: 2001
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Article
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC1728268/
https://ncbi.nlm.nih.gov/pubmed/11302967
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/gut.48.5.671
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