Article
Mutations in SCG10 are not involved in Hirschsprung disease.
PloS one - 20 Dec 2010
Alves Maria M M, Osinga Jan, Verheij Joke B G M, Metzger Marco, Eggen Bart J L, Hofstra Robert M W
Abstract excerpt
Hirschsprung disease (HSCR) is a congenital malformation characterized by the absence of enteric neurons in the distal part of the colon. Several genes have been implicated in the development of this disease that together account for 20% of all cases, implying that other genes are involved. Since...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.