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Article

Mutation analysis of FANCD2, BRIP1/BACH1, LMO4 and SFN in familial breast cancer.

Breast cancer research : BCR - 1 Jan 2005

Lewis Aaron G, Flanagan James, Marsh Anna, Pupo Gulietta M, Mann Graham, Spurdle Amanda B, Lindeman Geoffrey J, Visvader Jane E, Brown Melissa A, Chenevix-Trench Georgia

Abstract excerpt

INTRODUCTION: Mutations in known predisposition genes account for only about a third of all multiple-case breast cancer families. We hypothesized that germline mutations in FANCD2, BRIP1/BACH1, LMO4 and SFN may account for some of the unexplained multiple-case breast cancer families. METHODS: The families used in this study were ascertained through the Kathleen Cuningham Foundation Consortium for Research into...

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Source

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Identifiers

PMID: 16280053
DOI: 10.1186/bcr1336
PMCID: PMC1410737

Genes

BACH1
FANCD2
BRIP1
LMO4
SFN
BRCA1

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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