Association study of PHOX2B as a candidate gene for Hirschsprung’s disease

Background: Hirschsprung’s disease (HSCR) is a congenital disorder characterised by an absence of ganglion cells in the nerve plexuses of the lower digestive tract. Manifestation of the disease has been linked to mutations in genes that encode the crucial signals for the development of the enteric n...

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Main Authors: Garcia-Barceló, M, Sham, M H, Lui, V C H, Chen, B L S, Ott, J, Tam, P K H
Formato: Artigo
Idioma:Inglês
Publicado em: Copyright 2003 by Gut 2003
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Colon
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1773584/
https://ncbi.nlm.nih.gov/pubmed/12631670
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