Four Novel Polymorphisms in the Fibrinogen Aα Gene

• References

• 1 Bentolila S, Samama MM, Conard J, Horellou MH, Ffrench P. Dysfibrino-genaemia and thrombosis - report of a family (Fibrinogen Melun) and review of the literature. Ann Med Intern 1995; 146: 575-80.
• 2 Uemichi T, Liepnieks JJ, Benson MD. Hereditary renal amyloidosis with a novel variant fibrinogen. J Clin Invest 1994; 93: 731-6.
• 3 Brennan SO, Wyatt JM, Medicina D, Callea PMGeorge. Fibrinogen Brescia: Hepatic endoplasmic reticulum storage and hypofibrinogenemia because of a γ284 Gly→Arg mutation. Am J Pathol 2000; 157: 189-96.
• 4 Humphries SE, Luong LA, Montgomery HE, Day INM, Mohamed-Ali V, Mohamed-Ali V, Yudkin JS. Gene-environment interaction in the determination of levels of plasma fibrinogen. Thromb Haemost 1999; 82: 818-25.
• 5 Menegatti M, Asselta R, Duga S, Malcovati M, Bucciarelli P, Mannucci PM, Tenchini ML. Identification of Four Novel Polymorphisms in the Aalpha and gamma Fibrinogen Genes and Analysis of Association with Plasma Levels of the Protein. Thromb Res 2001; 103: 299-307.
• 6 Remijn JA, van Wijk R, de Groot PG. et al. Nature of the fibrinogen A alpha gene TaqI polymorphism. Thromb Haemost 2001; 86 (03) 935-6.
• 7 Humphries SE, Imam AM, Robbins TP, Cook M, Carritt B, Ingle C, Williamson R. The identification of a DNA polymorphism of the a fibrinogen gene, and the regional assignment of the human fibrinogen genes to 4q26-qter. Hum Genet 1984; 68: 148-53.
• 8 Banchs I, Bosch A, Guimera J, Lazaro C, Puig A, Estivill X. New alleles at microsatellite loci in CEPH families mainly arise from somatic mutations in the lymphoblastoid cell lines. Hum Mutat 1994; 03: 365-72.