A brief communication of patients with homozygous C282Y mutation-related hereditary hemochromatosis
A brief communication of patients with homozygous C282Y mutation-related hereditary hemochromatosis
About this item
Full title
Author / Creator
Publisher
Turkey: Kare Publishing
Journal title
Language
English
Formats
Publication information
Publisher
Turkey: Kare Publishing
Subjects
More information
Scope and Contents
Contents
Hereditary hemochromatosis (HH) is an autosomal recessive inherited iron-loading disorder and is characterized by chronic hepatitis, cirrhosis, diabetes, and bronze skin. The hemochromatosis gene (C282Y homozygosity)-related hemochromatosis is the most common form of HH. The prevalence of HH is varied. Here, we defined six cases with C282Y homozygo...
Alternative Titles
Full title
A brief communication of patients with homozygous C282Y mutation-related hereditary hemochromatosis
Authors, Artists and Contributors
Author / Creator
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_11237243
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_11237243
Other Identifiers
ISSN
2757-7392,1307-5888
E-ISSN
2757-7392
DOI
10.14744/hf.2024.2024.0020