Hepatocellular carcinoma and the penetrance of HFE C282Y mutations: a cross sectional study

BACKGROUND: Although most patients with hereditary haemochromatosis have HFE C282Y mutations, the lifetime risk to HFE C282Y homozygotes of developing fatal diseases such as hepatocellular carcinoma is uncertain. We have carried out a cross-sectional study to determine the proportion of diagnosed he...

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Detalles Bibliográficos
Autores principales: Willis, Gavin, Bardsley, Vicky, Fellows, Ian W, Lonsdale, Ray, Wimperis, Jennie Z, Jennings, Barbara A
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2005
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1175847/
https://www.ncbi.nlm.nih.gov/pubmed/15929796
http://dx.doi.org/10.1186/1471-230X-5-17

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1175847/
https://www.ncbi.nlm.nih.gov/pubmed/15929796
http://dx.doi.org/10.1186/1471-230X-5-17

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