Article
Hemochromatosis gene (HFE) mutations in South East Asia: a potential for iron overload.
Blood cells, molecules & diseases - 1 Jan 2000
Pointon Jennifer J, Viprakasit Vip, Miles Katie L, Livesey Karen J, Steiner Michael, O'Riordan Sean, Hien Tran T, Merryweather-Clarke Alison T, Robson Kathryn J H
Abstract excerpt
Hereditary hemochromatosis (HH) is an autosomal recessive disease caused by mutations in the HFE gene that mainly affects populations of European descent. Recently a novel mutation (IVS5+1 G-->A) has been described in a Vietnamese patient with HH that was not detected in a European control population. We have developed a novel method to screen for this mutation based on restriction enzyme digestion of a PCR...
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