Fanconi anemia, complementation group F [Homo sapiens]

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FANCF hypomethylation is associated with colorectal cancer in Han Chinese. [Turk J Gastroenterol. 2020]
FANCF hypomethylation is associated with colorectal cancer in Han Chinese.
Yu H, Pan R, Gao T, Wu D, Ying J, Duan S. Turk J Gastroenterol. 2020 Aug; 31(8):558-565.
A novel frame-shift deletion in FANCF gene causing autosomal recessive Fanconi anemia: a case report. [BMC Med Genet. 2019]
A novel frame-shift deletion in FANCF gene causing autosomal recessive Fanconi anemia: a case report.
Zareifar S, Dastsooz H, Shahriari M, Faghihi MA, Shekarkhar G, Bordbar M, Zekavat OR, Shakibazad N. BMC Med Genet. 2019 Jul 9; 20(1):122. Epub 2019 Jul 9.
Phenotypic variability in patients with Fanconi anemia and biallelic FANCF mutations. [Am J Med Genet A. 2017]
Phenotypic variability in patients with Fanconi anemia and biallelic FANCF mutations.
Tryon R, Zierhut H, MacMillan ML, Wagner JE. Am J Med Genet A. 2017 Jan; 173(1):260-263. Epub 2016 Oct 7.

RefSeq genomic sequence
See the genomic reference sequence for the FANCF gene (NG_007425.1).
RefSeq protein
See the reference protein sequence for Fanconi anemia group F protein (NP_073562.1).

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Fanconi anemia, complementation group F [Homo sapiens]
Fanconi anemia, complementation group F [Homo sapiens]
gi|55249547|gb|AAH47028.1|

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