Iranian hereditary hemochromatosis patients: Baseline characteristics, laboratory data and gene mutations

BACKGROUND: Hereditary hemochromatosis (HH) is the most common autosomal recessive disorder in white people, characterized by highly abnormal uptake of iron from the gastrointestinal tracts. Recently, mutation studies have focused to detect the genes responsible for HH. MATERIAL/METHODS: In this cro...

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Detalles Bibliográficos
Autores principales: Zamani, Farhad, Bagheri, Zohreh, Bayat, Maryam, Fereshtehnejad, Seyed-Mohammad, Basi, Ali, Najmabadi, Hossein, Ajdarkosh, Hossein
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2012
Materias:
Clinical Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3560564/
https://www.ncbi.nlm.nih.gov/pubmed/23018356
http://dx.doi.org/10.12659/MSM.883489

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3560564/
https://www.ncbi.nlm.nih.gov/pubmed/23018356
http://dx.doi.org/10.12659/MSM.883489

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