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Article

The Fanconi anaemia genome stability and tumour suppressor network.

Mutagenesis - 1 Nov 2002

Bogliolo M, Cabré O, Callén E, Castillo V, Creus A, Marcos R, Surrallés J

Abstract excerpt

Fanconi anaemia (FA) is a rare autosomal recessive disease characterized by increased spontaneous and DNA crosslinker-induced chromosome instability, progressive pancytopenia and cancer susceptibility. An increasing number of genes are involved in FA, including the breast cancer susceptibility ge...

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Source

Identifiers

PMID: 12435850
DOI: 10.1093/mutage/17.6.529

Genes

FANCD2
ATM
BRCA1
BRCA2
FANCA
FANCC
FANCE
FANCF
FANCG

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-12435850-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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