Comprehensive analysis of genotypes and phenotypes in 23 Chinese patients with hemophilia B: Identification of five novel variants-Reference-Cited by-同舟云学术

Comprehensive analysis of genotypes and phenotypes in 23 Chinese patients with hemophilia B: Identification of five novel variants

Published:2022-12-27 Issue: Volume: Page:
ISSN:1751-5521
Container-title:International Journal of Laboratory Hematology
language:en
Short-container-title:Int J Lab Hematology

Author:

Lu Linna¹^ORCID,Zhang Xialin²,Ren Juan¹^ORCID,Liu Xiue¹,Zhang Ruijuan²,Yang Linhua¹^ORCID,Wang Gang¹^ORCID

Affiliation:

1. Institute of Hematology The Second Hospital of Shanxi Medical University Taiyuan People's Republic of China

2. Department of Hematology, Shanxi Bethune Hospital, Shanxi Academy of Medical Sciences, Tongji Shanxi Hospital Third Hospital of Shanxi Medical University Taiyuan People's Republic of China

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Biochemistry (medical),Clinical Biochemistry,Hematology,General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/ijlh.14013

Reference12 articles.

1. WFH Guidelines for the Management of Hemophilia, 3rd edition

2. The Molecular Basis of FIX Deficiency in Hemophilia B

3. Human coagulation factor IX: a systematic review of its characteristics

4. X-ray structure of clotting factor IXa: active site and module structure related to Xase activity and hemophilia B.

5. When a ribosome encounters a premature termination codon

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