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
✦ LIBER ✦
Hereditary spherocytosis associated with mutations in HFE gene
✍ Scribed by M.A. Montes-Cano; F. Rodríguez-Muñoz; R. Franco-Osorio; A. Núñez-Roldán; M.F. González-Escribano
- Publisher
- Springer
- Year
- 2003
- Tongue
- English
- Weight
- 154 KB
- Volume
- 82
- Category
- Article
- ISSN
- 0939-5555
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