Genotypic and phenotypic spectra of hemojuvelin mutations in primary hemochromatosis patients: a systematic review

Hereditary hemochromatosis (HH) is a genetic disorder that causes excess absorption of iron and can lead to a variety of complications including liver cirrhosis, arthritis, abnormal skin pigmentation, cardiomyopathy, hypogonadism, and diabetes. Hemojuvelin (HJV) is the causative gene of a rare subty...

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Detalles Bibliográficos
Autores principales: Kong, Xiaomu, Xie, Lingding, Zhu, Haiqing, Song, Lulu, Xing, Xiaoyan, Yang, Wenying, Chen, Xiaoping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6615163/
https://www.ncbi.nlm.nih.gov/pubmed/31286966
http://dx.doi.org/10.1186/s13023-019-1097-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6615163/
https://www.ncbi.nlm.nih.gov/pubmed/31286966
http://dx.doi.org/10.1186/s13023-019-1097-2

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