Type 4B hereditary hemochromatosis associated with a novel mutation in the SLC40A1 gene: A case report and a review of the literature

RATIONALE: Hereditary hemochromatosis can be divided into HFE- and non-HFE-related based on genetic mutations in different genes. HFE-related hemochromatosis is the most common inherited genetic disease in European populations but rare in Asia-pacific region. Recently, non-HFE-related hemochromatosi...

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Detalles Bibliográficos
Autores principales: Zhang, Wei, Lv, Tingxia, Huang, Jian, Ou, Xiaojuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2017
Materias:
4500
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5617709/
https://www.ncbi.nlm.nih.gov/pubmed/28930842
http://dx.doi.org/10.1097/MD.0000000000008064

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5617709/
https://www.ncbi.nlm.nih.gov/pubmed/28930842
http://dx.doi.org/10.1097/MD.0000000000008064

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