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The First Case of Acute Myeloid Leukemia With Underlying Fanconi Anemia due to FANCF Variants in Korea
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참고문헌 (9)
- Arber DA, "The 2016 revision to the World Health Organization classification of myeloid neoplasms and acute leukemia", Blood, 127, pp.2391~2405 (2016)
- Mehta PA, "GeneReviews" (2002), University of Washington
- de Winter JP, "The Fanconi anaemia gene FANCF encodes a novel protein with homology to ROM", Nat Genet, 24, pp.15~16 (2000)
- Nicchia E, "Clinical aspects of Fanconi anemia individuals with the same mutation of FANCF identified by next generation sequencing", Birth Defects Res A Clin Mol Teratol, 103, pp.1003~1010 (2015)
- Tryon R, "Phenotypic variability in patients with Fanconi anemia and biallelic FANCF mutations", Am J Med Genet A, 173, pp.260~263 (2017)
- Zareifar S, "A novel frame-shift deletion in FANCF gene causing autosomal recessive Fanconi anemia : a case report", BMC Med Genet, 20, pp.122~ (2019)
- Del Valle J, "Exploring the role of mutations in Fanconi anemia genes in hereditary cancer patients", Cancers(Basel), 12, pp.829~ (2020)
- Richards S, "Standards and guidelines for the interpretation of sequence variants : a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology", Genet Med, 17, pp.405~424 (2015)
- Giardino S, "Outcome of patients with Fanconi anemia developing myelodysplasia and acute leukemia who received allogeneic hematopoietic stem cell transplantation : a retrospective analysis on behalf of EBMT group", Am J Hematol, 95, pp.809~816 (2020)
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