Haemophilia B: database of point mutations and short additions and deletions-Reference-Cited by-同舟云学术

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Haemophilia B: database of point mutations and short additions and deletions

Published:1990 Issue:14 Volume:18 Page:4053-4059
ISSN:0305-1048
Container-title:Nucleic Acids Research
language:en
Short-container-title:Nucl Acids Res

Author:

Giannelli F.,Green P. M.,High K. A.,Lozier J. N.,Lillicrap D. P.,Ludwig M.,Olek K.,Reitsma P. H.,Goossens M.,Yoshioka A.,Sommer S.,Brownlee G. G.

Publisher

Oxford University Press (OUP)

Subject

Genetics

Link

http://academic.oup.com/nar/article-pdf/18/14/4053/7077806/18-14-4053.pdf

Cited by 68 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. Study on the Mutation of FⅨ Gene in 31 Patients with Type B Hemophilia;Clinical and Applied Thrombosis/Hemostasis;2024-01

2. F8/F9 variants in the population-based PedNet Registry cohort compared with locus-specific genetic databases of the European Association for Haemophilia and Allied Disorders and the Centers for Disease Control and Prevention Hemophilia A or Hemophilia B Mutation Project;Research and Practice in Thrombosis and Haemostasis;2023-01

3. The EAHAD blood coagulation factor VII variant database;Human Mutation;2020-04-29

4. The European Association for Haemophilia and Allied Disorders (EAHAD) Coagulation Factor Variant Databases: Important resources for haemostasis clinicians and researchers;Haemophilia;2020-03

5. Furin‐mediated protein processing in infectious diseases and cancer;Clinical & Translational Immunology;2019-01

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