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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...
में बचाया:
| मुख्य लेखकों: | , , , |
|---|---|
| स्वरूप: | Artigo |
| भाषा: | Inglês |
| प्रकाशित: |
BioMed Central
2006
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| विषय: | |
| ऑनलाइन पहुंच: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1468397/ https://ncbi.nlm.nih.gov/pubmed/16672055 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2350-7-43 |
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