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Polymorphism of theHFEGene Associated with Hereditary Hemochromatosis in Populations of Russia

✍ Scribed by S. V. Mikhailova; V. F. Kobzev; I. V. Kulikov; A. G. Romaschenko; V. I. Khasnulin; M. I. Voevoda

Book ID: 111544937
Publisher: SP MAIK Nauka/Interperiodica
Year: 2003
Tongue: English
Weight: 122 KB
Volume: 39
Category: Article
ISSN: 1022-7954
DOI: 10.1023/a:1024765406867

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Homozygosity for the mutation Cys282Tyr in the HFE gene has recently been identified as a cause of hereditary hemochromatosis, a disorder resulting in the inappropriate absorption of iron. Approximately 10% of Caucasians are heterozygous for this mutation; however, the gene frequency in African Amer