Hirschsprung disease is associated with an L286P mutation in the fifth transmembrane domain of the endothelin-B receptor in the N-ethyl-N-nitrosourea-induced mutant line

Hirschsprung disease (HSCR), or colonic aganglionosis, is a congenital disorder characterized by the absence of intramural ganglia along variable lengths of the colon, resulting in intestinal obstruction. It is the most common cause of congenital intestinal obstruction, with an incidence of 1 in 5,0...

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Bibliographische Detailangaben
Veröffentlicht in:Exp Anim
Hauptverfasser: Chen, Bing, Ouyang, Hui-Ling, Wang, Wen-Hua, Yin, Yi-Heng, Yan, Lin-Na, Yang, Bin, Xue, Zheng-Feng
Format: Artigo
Sprache:Inglês
Veröffentlicht: Japanese Association for Laboratory Animal Science 2016
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Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4976238/
https://ncbi.nlm.nih.gov/pubmed/26923755
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1538/expanim.15-0110
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