Genetic analysis of a compound heterozygous patient with congenital factor X deficiency and regular replacement therapy with a prothrombin complex concentrate-Reference-Cited by-同舟云学术

Genetic analysis of a compound heterozygous patient with congenital factor X deficiency and regular replacement therapy with a prothrombin complex concentrate

Published:2019-10-30 Issue:1 Volume:111 Page:51-56
ISSN:0925-5710
Container-title:International Journal of Hematology
language:en
Short-container-title:Int J Hematol

Author:

Togashi Tomoki,Nagaya Satomi,Nagasawa Masayuki,Meguro-Horike Makiko,Nogami Keiji,Imai Yuta,Kuzasa Kana,Sekiya Akiko,Horike Shin-ichi,Asakura Hidesaku,Morishita Eriko^ORCID

Funder

the Ministry of Health, Labor and Welfare of Japan

the Ministry of Education, Culture, Sports, Science and Technology of Japan

Japan Agency for Medical Research and Development

Publisher

Springer Science and Business Media LLC

Subject

Hematology

Link

http://link.springer.com/content/pdf/10.1007/s12185-019-02767-y.pdf

Reference19 articles.

1. Nagaya S, Akiyama M, Murakami M, Sekiya A, Asakura H, Morishita E. Congenital coagulation factor X deficiency: Genetic analysis of five patients and functional characterization of mutant factor X proteins. Haemophilia. 2018;24:774–85.