A case report of hereditary hemochromatosis caused by mutation of SLC40A1 gene

RATIONALE: Hereditary hemochromatosis (HH) is a frequent autosomal recessive disease. The pathogenesis of disease is excessive intestinal absorption of dietary iron, resulting in pathologically high iron storage in tissues and organs. As a systemic disease, it has several manifestations including ci...

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Detalles Bibliográficos
Autores principales: Yin, Xin, Zhang, Yu, Gao, Hui, Jin, Qing-long, Wen, Xiao-yu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2019
Materias:
4500
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6946363/
https://www.ncbi.nlm.nih.gov/pubmed/31689754
http://dx.doi.org/10.1097/MD.0000000000017526

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6946363/
https://www.ncbi.nlm.nih.gov/pubmed/31689754
http://dx.doi.org/10.1097/MD.0000000000017526

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