Abstract
Mutations of the HJV gene, which maps on chromosome 1q21, underlie most cases of juvenile hemochromatosis. We evaluated the frequency of the most common mutation (G320V) of the HJV gene in the Greek population, since 50% of cases of hereditary hemochromatosis in Greece carry mutations of the HJV gene.
Vol. 89 No. 6 (2004): June, 2004 : Letters to the Editor
Published By
Ferrata Storti Foundation, Pavia, Italy
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