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Article

Hemochromatosis (HFE) and transferrin receptor-1 (TFRC1) genes in sporadic porphyria cutanea tarda (sPCT).

Cellular and molecular biology (Noisy-le-Grand, France) - 1 Feb 2002

Lamoril Jérĵme, Andant Christophe, Gouya Laurent, Malonova Eva, Grandchamp Bernard, Martásek Pavel, Deybac Jean-Charles, Puy Hervé

Abstract excerpt

Porphyria cutanea tarda (PCT), a disorder characterized by a photosensitive dermatosis and hepatic siderosis, is caused by a decreased activity of the hepatic enzyme uroporphyrinogen decarboxylase (UROD). Two forms of PCT have been described: a familial one (fPCT) with an inherited decrease of UROD activity in all tissues and a sporadic one (sPCT) with a decreased UROD activity restricted to the liver. Iron...

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Source

Identifiers

PMID: 11929045

Genes

HFE
UROD

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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Hemochromatosis (HFE) and transferrin receptor-1 (TFRC1) genes in sporadic porphyria cutanea tarda (sPCT).PMID 11929045Read ↗

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