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Article

Comprehensive cytochrome P450 CYP1A2 gene analysis in French caucasian patients with familial and sporadic porphyria cutanea tarda.

The British journal of dermatology - 1 Feb 2012

Tchernitchko D, Robréau A M, Lefebvre T, Lamoril J, Deybach J C, Puy H

Abstract excerpt

BACKGROUND: Porphyria cutanea tarda (PCT), the most frequent type of porphyria, results from decreased uroporphyrinogen decarboxylase (UROD) activity. Two forms of PCT have been described: a familial form (fPCT) characterized by the inherited decrease of UROD activity in all tissues and a sporadic form (sPCT) characterized by decreased UROD activity in the liver. Cytochrome P450 CYP1A2 plays a major role in...

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Source

Identifiers

PMID: 21929532
DOI: 10.1111/j.1365-2133.2011.10642.x

Genes

UROD

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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