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Haemochromatosis gene mutation in hepatocellular cancer
Willis et al used a genetic test to estimate the incidence of hepatocellular cancer among 3,600 individuals predicted to be homozygous for the HLA-H nucleotide 845G to A mutation. The penetrance of the 845A homozygous genotype is low with respect to hepatocellular cancer in this population.
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Published in: | The Lancet (British edition) 1997-08, Vol.350 (9077), p.565-566 |
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creator | Willis, G Wimperis, JZ Lonsdale, R Jennings, BA |
description | Willis et al used a genetic test to estimate the incidence of hepatocellular cancer among 3,600 individuals predicted to be homozygous for the HLA-H nucleotide 845G to A mutation. The penetrance of the 845A homozygous genotype is low with respect to hepatocellular cancer in this population. |
doi_str_mv | 10.1016/S0140-6736(05)63143-1 |
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subjects | Biological and medical sciences Cancer Carcinoma, Hepatocellular - genetics Gastroenterology. Liver. Pancreas. Abdomen Genes Genotype Hemochromatosis - genetics Hemochromatosis Protein Histocompatibility Antigens Class I - genetics HLA Antigens - genetics Humans Liver Liver Neoplasms - genetics Liver. Biliary tract. Portal circulation. Exocrine pancreas Medical sciences Membrane Proteins Mutation Tumors |
title | Haemochromatosis gene mutation in hepatocellular cancer |
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