ISSN:
1546-1718
Source:
Nature Archives 1869 - 2009
Topics:
Biology
,
Medicine
Notes:
[Auszug] Hirschsprung disease (HSCR) is a multigenic, congenital disorder that affects 1 in 5,000 newborns and is characterized by the absence of neural crest–derived enteric ganglia in the colon. One of the primary genes affected in HSCR encodes the G protein–coupled endothelin receptor-B ...
Type of Medium:
Electronic Resource
URL:
http://dx.doi.org/10.1038/ng1371
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