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Mutation analysis of the HFE gene in hereditary hemochromatosis

✍ Scribed by Ocran, Kenneth; Buettner, Carsten A.; Genschel, Janine; Steiner, Michael; Schneider, Marie-Luise; Gert, Helga; Charite Mitte, Campus; Schuff-Werner, P.; Kerner, W.; Lochs, Herbert; Schmidt, Hartmut Hj


Book ID
124112575
Publisher
Elsevier Science
Year
2001
Tongue
English
Weight
186 KB
Volume
120
Category
Article
ISSN
0016-5085

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Mutation analysis of the HFE gene associ
✍ Monaghan, Kristin G.; Rybicki, Benjamin A.; Shurafa, Muhammad; Feldman, Gerald L πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 155 KB πŸ‘ 2 views

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