A combined syndrome of juvenile polyposis and hereditary haemorrhagic telangiectasia associated with mutations in MADH4 (SMAD4). [electronic resource]
- Lancet (London, England) Mar 2004
- 852-9 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
1474-547X
10.1016/S0140-6736(04)15732-2 doi
Adenomatous Polyposis Coli--epidemiology Comorbidity DNA-Binding Proteins--genetics Gene Expression--genetics Humans Mutation Phenotype Signal Transduction--genetics Smad4 Protein Syndrome Telangiectasia, Hereditary Hemorrhagic--epidemiology Trans-Activators--genetics