FVIII p.Arg1800His mutation is associated with mild/moderate hemophilia A in Chinese population-Reference-Cited by-同舟云学术

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FVIII p.Arg1800His mutation is associated with mild/moderate hemophilia A in Chinese population

Published:2018-05-13 Issue:5 Volume:40 Page:e90-e92
ISSN:1751-5521
Container-title:International Journal of Laboratory Hematology
language:en
Short-container-title:Int J Lab Hem

Author:

Wang X.¹,Lyu Y.²,Shen N.¹,Hu Q.³,Lu Y.¹^ORCID

Affiliation:

1. Department of Laboratory Medicine; Tongji Hospital; Tongji Medical College; Huazhong University of Science and Technology; Wuhan China

2. Department of Cardiology; Renmin Hospital of Wuhan University; Wuhan China

3. Department of Pediatrics; Tongji Hospital; Tongji Medical College; Huazhong University of Science and Technology; Wuhan China

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Biochemistry, medical,Clinical Biochemistry,Hematology,General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/ijlh.12851/fullpdf

Reference12 articles.

1. Haemophilias A and B;Bolton-Maggs;Lancet,2003

2. A domain mutations in 65 haemophilia A families and molecular modelling of dysfunctional factor VIII proteins;Liu;Br J Haematol,1998

3. Characterization of mutations within the factor VIII gene of 73 unrelated mild and moderate haemophiliacs;Schwaab;Br J Haematol,1995

4. Molecular characterization of severe hemophilia A suggests that about half the mutations are not within the coding regions and splice junctions of the factor VIII gene;Higuchi;Proc Natl Acad Sci USA,1991

5. Mutation spectrum of 122 hemophilia A families from Taiwanese population by LD-PCR, DHPLC, multiplex PCR and evaluating the clinical application of HRM;Lin;BMC Med Genet,2008

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Hemophagocytic lymphohistiocytosis and congenital factor VII deficiency: a case report;BMC Medical Genetics;2018-09-12

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