The prevalence of heterozygous F12 mutations in Chinese population and its relevance to incidents of thrombosis
Author:
Funder
National Natural Science Foundation of China
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1186/s12881-018-0557-1.pdf
Reference20 articles.
1. Ramot B, Singer K, Heller P, Zimmerman HJ. Hageman factor (HF) deficiency. Blood. 1956;11(8):745–52.
2. Lämmle BWW, Huber I, Krauskopf M, Zürcher C, Pflugshaupt R, Furlan M. Thromboembolism and bleeding tendency in congenital factor XII deficiency--a study on 74 subjects from 14 Swiss families. Thromb Haemost. 1991;65(2):117–21.
3. Koster T, Rosendaal FR, Briet E, Vandenbroucke JP. John Hageman’s factor and deep-vein thrombosis: Leiden thrombophilia study. Br J Haematol. 1994;87(2):422–4.
4. Girolami A, Randi ML, Gavasso S, Lombardi AM, Spiezia F. The occasional venous thromboses seen in patients with severe (homozygous) FXII deficiency are probably due to associated risk factors: a study of prevalence in 21 patients and review of the literature. J Thromb Thrombolysis. 2004;17(2):139–43.
5. Schloesser M, et al. Mutations in the human factor XII gene. Blood. 1997;90(10):3967–77.
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