Coagulation Testing in the Core Laboratory.
Winter WE, Flax SD, Harris NS.
Lab Med. 2017 Nov 8;48(4):295-313. doi: 10.1093/labmed/lmx050.
Haploinsufficiency of A20.
Deuitch NT, Schwartz DM, Aksentijevich I.
2024 Dec 19. In: Adam MP, Bick S, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2026.
Fibrinogen Aalpha gene genotyping in patients with inherited afibrinogenemia deficiency; a novel mutation in Iranian afibrinogenemia patients.
Moazzeni A, Naderi M, Dorgalaleh A, Alizadeh S.
Blood Coagul Fibrinolysis. 2023 Dec 1;34(8):517-522. doi: 10.1097/MBC.0000000000001260. Epub 2023 Oct 10.
Congenital Fibrinogen Deficiency in India and Role of Human Fibrinogen Concentrate.
John MJ, Byreddy P, Modak K, Makkar M.
Acta Haematol. 2021;144(6):595-602. doi: 10.1159/000516339. Epub 2021 Jun 4.
Rare bleeding disorders: Advances in management.
Casini A, Al-Samkari H, Hayward C, Peyvandi F.
Haemophilia. 2024 Apr;30 Suppl 3:60-69. doi: 10.1111/hae.14986. Epub 2024 Mar 18.
Pseudohomozygous dysfibrinogenemia.
Peck RC, Fitzgibbon L, Reilly-Stitt C, Doherty C, Phillips E, Mumford AD.
Res Pract Thromb Haemost. 2021 Aug 21;5(6):e12568. doi: 10.1002/rth2.12568. eCollection 2021 Aug.
Thromboembolic events in patients with severe inherited fibrinogen deficiency.
Rottenstreich A, Lask A, Schliamser L, Zivelin A, Seligsohn U, Kalish Y.
J Thromb Thrombolysis. 2016 Aug;42(2):261-6. doi: 10.1007/s11239-015-1325-0.
[Phenotype and genotype analyses of two pedigrees with inherited fibrinogen deficiency].
Jia KQ, Su ZX, Chen HL, Zheng XY, Zeng ML, Zhang K, Ye LY, Yang LL, Jin YH, Wang MS.
Zhonghua Xue Ye Xue Za Zhi. 2023 Nov 14;44(11):930-935. doi: 10.3760/cma.j.issn.0253-2727.2023.11.008.
Rare inherited disorders of fibrinogen.
Acharya SS, Dimichele DM.
Haemophilia. 2008 Nov;14(6):1151-8. doi: 10.1111/j.1365-2516.2008.01831.x.
Molecular basis of fibrinogen deficiency.
Neerman-Arbez M.
Pathophysiol Haemost Thromb. 2006;35(1-2):187-98. doi: 10.1159/000093566.
