Role of RET and PHOX2B gene polymorphisms in risk of Hirschsprung's disease in Chinese population
AUTOR(ES)
Miao, Xiaoping
FONTE
BMJ Group
ACESSO AO ARTIGO
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=1942142Documentos Relacionados
- Molecular heterogeneity of RET loss of function in Hirschsprung's disease.
- Various mechanisms cause RET-mediated signaling defects in Hirschsprung's disease.
- Long segment and short segment familial Hirschsprung's disease: variable clinical expression at the RET locus.
- Central hypoventilation with PHOX2B expansion mutation presenting in adulthood
- Hirschsprung's Disease and Congenital Deafness