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Frequency of common HFE variants in the Saudi population: a high throughput molecular beacon-based study
BACKGROUND: Hereditary Hemochromatosis (HH) is an autosomal recessive disorder highlighted byiron-overload. Two popular mutations in HFE, p.C282Y and p.H63D, have been discovered and found to associate with HH in different ethnic backgrounds. p.C282Y and p.H63D diagnosis is usually made byrestrictio...
| Autores principales: | , , , |
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| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2006
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1468397/ https://www.ncbi.nlm.nih.gov/pubmed/16672055 http://dx.doi.org/10.1186/1471-2350-7-43 |