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Article

Characterization of molecular defects in xeroderma pigmentosum group C.

Nature genetics - 1 Dec 1993

Li L, Bales E S, Peterson C A, Legerski R J

Abstract excerpt

Xeroderma pigmentosum (XP) is a rare autosomal recessive disease of humans characterized by an accelerated chronic degeneration of sun-exposed areas of the body, including an elevated risk of developing cancers of the skin. We recently reported the isolation of a gene XPCC that complements the repair deficiency of cultured XP-C cells. Here we report the results of a characterization of XPCC at the nucleotide...

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Identifiers

PMID: 8298653
DOI: 10.1038/ng1293-413

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

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Characterization of molecular defects in xeroderma pigmentosum group C.PMID 8298653Read ↗

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Structural and mutational analysis of the xeroderma pigmentosum group D (XPD) gene.Semantic proximity Read ↗

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