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Article

[Progress of research on protein composition and gene therapy of Fanconi anaemia - review].

Zhongguo shi yan xue ye xue za zhi - 1 Apr 2004

Li Zai-Yi, Zou Yi-Feng, Deng Yu-Bin

Abstract excerpt

Fanconi anaemia (FA) is an autosomal recessive inherited disorder caused by defects in hematopoietic stem cells. The clinical manifestations of FA are diverse and complicated. FA cells display high hypersensitivity to agents which produce interstrand DNA cross-links such as mitomycin C (MMC) or diepoxybutane (DEB). At least eight complementation groups with defects in eight genes (FANCA, FANCB, FANCC, FANCD(1),...

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Source

Identifiers

PMID: 15157341

Genes

FANCA
FANCB
FANCC
FANCE
FANCF
FANCG

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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