HFE protein impact on iron metabolism

Hereditary hemochromatosis type 1 is an autosomal recessive disorder caused by HFE gene mutations, which is an iron homeostasis metabolism controlling co-factor. Adults with male predomination present with clinical symptoms derived by iron overload in organs. The phenotype expression is individual w...

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Detalles Bibliográficos
Autores principales: Kaczorowska-Hać, Barbara, Kaczor, Jan Jacek
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sciendo 2017
Materias:
Review Article/Praca Poglądowa
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8522971/
https://www.ncbi.nlm.nih.gov/pubmed/28796976
http://dx.doi.org/10.34763/devperiodmed.20172102.8590

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8522971/
https://www.ncbi.nlm.nih.gov/pubmed/28796976
http://dx.doi.org/10.34763/devperiodmed.20172102.8590

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