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Article

Sequence variation in the Fanconi anemia gene FAA.

Proceedings of the National Academy of Sciences of the United States of America - 25 Nov 1997

Levran O, Erlich T, Magdalena N, Gregory J J, Batish S D, Verlander P C, Auerbach A D

Abstract excerpt

Fanconi anemia (FA) is a genetically heterogeneous autosomal recessive syndrome associated with chromosomal instability, hypersensitivity to DNA crosslinking agents, and predisposition to malignancy. The gene for FA complementation group A (FAA) recently has been cloned. The cDNA is predicted to encode a polypeptide of 1,455 amino acids, with no homologies to any known protein that might suggest a function for...

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Source

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Identifiers

PMID: 9371798
DOI: 10.1073/pnas.94.24.13051
PMCID: PMC24261

Genes

APC
BRCA1

Provenance

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

Source receipt: pubmed, retrieved 7 Sept 2026.

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