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Clinical Trial Summary

Hepatocellular carcinoma (HCC) is a frequent complication of cirrhosis. Occurrence of HCC could be linked with multiple functional region of genome. The determining of a genomic mapping of " single nucleotide polymorphisms " (SNPs) permit to perform some genetic link studies with pathologies without clear hereditary disposition. In this study, the investigators will identify predictives genetic polymorphism of HCC.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01065233
Study type Observational
Source Nantes University Hospital
Contact
Status Completed
Phase
Start date October 23, 2008
Completion date July 20, 2013

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