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...

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Detalles Bibliográficos
Autores principales: Alsmadi, Osama A, Al-Kayal, Fadi, Al-Hamed, Mohamed, Meyer, Brian F
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Research Article
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

Internet

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

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