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Related to FANCC: FANCG
FANCCFanconi Anemia, Complementation Group C
References in periodicals archive ?
The IVS4+4A>T mutation of the Fanconi anaemia gene FANCC is not associated with a severe phenotype in Japanese patients.
61 Abbreviations: ATM, ataxia telangiectasia-mutated; FANCC, Fanconi anemia complementation group C; UBC13, ubiquitin-conjugating enzyme 13; XPG, Xeroderma pigmentosum complementation group G; XRCC3, X-ray repair complementing defective repair in Chinese hamster cells 3.
3) La AF se asocia con alteracion en ocho genes, en donde el 70% de los pacientes tienen mutaciones en el gen FANCA, 10% en el gen FANCC, y el 10% en el gen FANCG; os otros genes rara vez se ven afectados.