Global prevalence of putative haemochromatosis mutations.

Author:

Merryweather-Clarke A T,Pointon J J,Shearman J D,Robson K J

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference33 articles.

1. The molecular basis of inherited disease;Bothwell, T.H.; Charlton, R.W.; Hemochromatosis, Motulsky A.G.,1995

2. Long-term survival in patients with hereditary hemochromatosis;Niederau, C.; Fischer, R.; Purschel, A.; Stremmel, W.; Haussinger, D.; Strohmeyer, G.;Gastroenterology,1996

3. Prevalence of iron overload in central Sweden;Olssen, K.S.; Ritter, B.; Rosen, U.; Heedman, P.A.; Staugard, F.;Acta Med Scand,1983

4. Prevalence of hemochromatosis among 11,065 presumably healthy blood donors;Edwards, C.Q.; Griffen, L.M.; Goldgar, D.; Drummond, C.; Skolnick, M.H.; Kushner, J.P.;N Engl J Med,1988

5. Mutation analysis in hereditary haemochromatosis;Beutler, E.; Gelbart, T.; West, C.;Blood Cells Mol Dis,1996

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