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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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Detaylı Bibliyografya
Asıl Yazarlar: Willis, Gavin, Bardsley, Vicky, Fellows, Ian W, Lonsdale, Ray, Wimperis, Jennie Z, Jennings, Barbara A
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: BioMed Central 2005
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC1175847/
https://ncbi.nlm.nih.gov/pubmed/15929796
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-230X-5-17
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