Association between C282Y and H63D mutations of the HFE gene with hepatocellular carcinoma in European populations: a meta-analysis

BACKGROUND: Hereditary hemochromatosis (HH) is an autosomal recessive disorder mainly associated with homozygosity for the C282Y and H63D mutations in the hemochromatosis (HFE) gene. The reports about the C282Y and H63D mutations and hepatocellular carninoma (HCC) were controversial. To clarify the...

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Detalles Bibliográficos
Autores principales: Jin, Fei, Qu, Li-Shuai, Shen, Xi-Zhong
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2845109/
https://www.ncbi.nlm.nih.gov/pubmed/20196837
http://dx.doi.org/10.1186/1756-9966-29-18

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2845109/
https://www.ncbi.nlm.nih.gov/pubmed/20196837
http://dx.doi.org/10.1186/1756-9966-29-18

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