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Article

Investigation of FANCA gene in Fanconi anaemia patients in Iran.

The Indian journal of medical research - 1 Feb 2016

Moghadam Ali Akbar Saffar, Mahjoubi Frouzandeh, Reisi Nahid, Vosough Parvaneh

Abstract excerpt

BACKGROUND & OBJECTIVES: Fanconi anaemia (FA) is a syndrome with a predisposition to bone marrow failure, congenital anomalies and malignancies. It is characterized by cellular hypersensitivity to cross-linking agents such as mitomycin C (MMC). In the present study, a new approach was selected to investigate FANCA (Fanconi anaemia complementation group A) gene in patients clinically diagnosed with cellular...

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Source

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Identifiers

PMID: 27121516
DOI: 10.4103/0971-5916.180206
PMCID: PMC4859127

Genes

FANCA

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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