H63/H63D genotype and the H63D allele are associated in patients with hyperferritinemia to the development of metabolic syndrome
Eur J Intern Med
.
2020 Feb:72:106-107.
doi: 10.1016/j.ejim.2019.11.021.
Epub 2019 Nov 30.
Authors
Agustin Castiella
1
,
Iratxe Urreta
2
,
Eva Zapata
3
,
M Dolores de Juan
4
,
Jose I Emparanza
2
;
Burnia Group
Affiliations
1
Gastroenterology Service, Donostia University Hospital, P. Dr Beguristain s/n, 20014 Donostia, Spain; Gastroenterology Service, Mendaro hospital, Mendaro, Spain. Electronic address:
[email protected]
.
2
Clinical Epidemiology Unit, CASPe, CIBER-ESP, Donostia University Hospital, P. Dr Beguristain s/n, 20014 Donostia, Spain.
3
Gastroenterology Service, Donostia University Hospital, P. Dr Beguristain s/n, 20014 Donostia, Spain.
4
Immunology Unit, Donostia University Hospital, P. Dr Beguristain s/n, 20014 Donostia, Spain.
PMID:
31796245
DOI:
10.1016/j.ejim.2019.11.021
No abstract available
Publication types
Letter
MeSH terms
Alleles
Gene Frequency
Genotype
Hemochromatosis Protein / genetics*
Hemochromatosis*
Humans
Hyperferritinemia*
Metabolic Syndrome* / genetics
Mutation
Substances
HFE protein, human
Hemochromatosis Protein