Frequency of Two Common HFE Gene Mutations (C282Y and H63D) in a Group of Iranian Patients With Cryptogenic Cirrhosis

BACKGROUND: The human HFE gene (a key component of iron homeostasis in humans) is involved in hereditary hemochromatosis, a common autosomal recessive genetic disorder that is characterized by excessive intestinal iron absorption and progressive iron overload. OBJECTIVES: In this study, we assessed...

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Detalles Bibliográficos
Autores principales: Jowkar, Zahra, Geramizadeh, Bita, Shariat, Mahmoud
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Kowsar 2011
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3269056/
https://www.ncbi.nlm.nih.gov/pubmed/22308152
http://dx.doi.org/10.5812/kowsar.1735143x.781

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3269056/
https://www.ncbi.nlm.nih.gov/pubmed/22308152
http://dx.doi.org/10.5812/kowsar.1735143x.781

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