Hereditary coagulation factor <scp>VII</scp> deficiency caused by novel compound heterozygous mutations in a Chinese pedigree: A case report-Reference-Cited by-同舟云学术

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Hereditary coagulation factor VII deficiency caused by novel compound heterozygous mutations in a Chinese pedigree: A case report

Published:2022-12-26 Issue:1 Volume:37 Page:
ISSN:0887-8013
Container-title:Journal of Clinical Laboratory Analysis
language:en
Short-container-title:Clinical Laboratory Analysis

Author:

Cai Ruimin¹^ORCID,Li Yi¹,Xu Wei¹,Gao Xue¹,Feng Qiang¹

Affiliation:

1. Department of Clinical Laboratory The Affiliated Taian City Central Hospital of Qingdao University Taian China

Publisher

Wiley

Subject

Microbiology (medical),Biochemistry (medical),Medical Laboratory Technology,Clinical Biochemistry,Public Health, Environmental and Occupational Health,Hematology,Immunology and Allergy

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jcla.24768

Reference16 articles.

1. Factor VII deficiency: defining the clinical picture and optimizing therapeutic options

2. Nucleotide sequence of the gene coding for human factor VII, a vitamin K-dependent protein participating in blood coagulation.

3. Macromolecular substrate affinity for free factor VIIa is independent of a buried protease domain N-terminus

4. Factor VII deficiency: clinical manifestation of 717 subjects from Europe and Latin America with mutations in the factor 7 gene

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