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Article

Sequencing analysis of SLX4/FANCP gene in Italian familial breast cancer cases.

PloS one - 1 Jan 2012

Catucci Irene, Colombo Mara, Verderio Paolo, Bernard Loris, Ficarazzi Filomena, Mariette Frederique, Barile Monica, Peissel Bernard, Cattaneo Elisa, Manoukian Siranoush, Radice Paolo, Peterlongo Paolo

Abstract excerpt

Breast cancer can be caused by germline mutations in several genes that are responsible for different hereditary cancer syndromes. Some of the genes causing the Fanconi anemia (FA) syndrome, such as BRCA2, BRIP1, PALB2, and RAD51C, are associated with high or moderate risk of developing breast cancer. Very recently, SLX4 has been established as a new FA gene raising the question of its implication in breast...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Open in PubMed Open full text

Identifiers

PMID: 22383991
DOI: 10.1371/journal.pone.0031038
PMCID: PMC3285620

Genes

SLX4
BRCA2
BRIP1
PALB2

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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Sequencing analysis of SLX4/FANCP gene in Italian familial breast cancer cases.PMID 22383991Read ↗

Analysis of the novel fanconi anemia gene SLX4/FANCP in familial breast cancer cases.Semantic proximity Read ↗

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Analysis of FANCB and FANCN/PALB2 fanconi anemia genes in BRCA1/2-negative Spanish breast cancer families.Semantic proximity Read ↗

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