References
- Shohat M, Halpern GJ. Familial Mediterranean fever-a review. Genet Med. 2011;13:487–498.
- Onen F. Familial Mediterranean fever. Rheumatol Int. 2006;26:489–496.
- Aslan D. Leukopenia in familial Mediterranean fever: case series and literature review with special emphasis on pathogenesis. Pediatr Hematol Oncol. 2014;31:120–128.
- Touitou I. The spectrum of familial Mediterranean fever (FMF) mutations. Eur J Hum Genet. 2001;9:473–483.
- Manukyan G, Aminov R. Update on pyrin functions and mechanisms of familial Mediterranean fever. Front Microbiol. 2016;7:456.
- Landrum MJ, Lee JM, Benson M, et al. ClinVar: improving access to variant interpretations and supporting evidence. Nucleic Acids Res. 2018;46:D1062–D1067.
- DePristo M, Banks E, Poplin R, et al. A framework for variation discovery and genotyping using next-generation DNA sequencing data. Nat Genet. 2011;43:491–498.
- Lek M, Karczewski KJ, Minikel EV, et al. Analysis of protein-coding genetic variation in 60,706 humans. Nature. 2016;536:285–291.
- Beyitler I, Kavukcu S. A case of familial Mediterranean fever having intermittent leukopenia. J Pediatr Hematol Oncol. 2018;40:e111–e112.
- Ganiou Tidjani K, Ailal F, Najib J, et al. Intermittent chronic neutropenia in a patient with familial Mediterranean fever. Pediatr Blood Cancer. 2008;51:701–703.
- Ben-Chetrit E, Navon P. Case report colchicine-induced leukopenia in a patient with familial Mediterranean fever: the cause and a possible approach. Clin Exp Rheumatol. 2003;21:S38–S40.
- Sakallioglu O. Leucopenia resoluted with colchicine in familial Mediterranean fever. J Pediatr Hematol Oncol. 2012;34:162.
- Mattit H, Joma M, Al-Cheikh S, et al. Familial Mediterranean fever in the Syrian population: gene mutation frequencies, carrier rates and phenotype–genotype correlation. Eur J of Med Genet. 2006;49:481–486.
- Booty MG, Chae JJ, Masters SL, et al. Familial Mediterranean fever with a single MEFV mutation: where is the second hit? Arthritis Rheum. 2009;60:1851–1861.
- Boycott KM, Vanstone MR, Bulman DE, et al. Rare-disease genetics in the era of next-generation sequencing: discovery to translation. Nat Rev Genet. 2013;14:681–691.