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Article

Mutations in HFE causing hemochromatosis are associated with primary hypertriglyceridemia.

The Journal of clinical endocrinology and metabolism - 1 Nov 2009

Solanas-Barca María, Mateo-Gallego Rocío, Calmarza Pilar, Jarauta Estíbaliz, Bea Ana M, Cenarro Ana, Civeira Fernando

Abstract excerpt

CONTEXT: Most cases of primary hypertriglyceridemia (HTG) are caused by the interaction of unknown polygenes and environmental factors. Elevated iron storage is associated with metabolic syndrome, diabetes, and obesity, and all of them are associated with HTG. OBJECTIVE: The aim of the study was to analyze whether HFE mutations causing hereditary hemochromatosis (HH) are associated with primary HTG. DESIGN:...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 19820015
DOI: 10.1210/jc.2009-0814

Genes

HFE

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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