Genotyping of the c.1423C>T (p.P475S) polymorphism in the ADAMTS13 gene by APLP and HRM assays: Northeastern Asian origin of the mutant
Author:
Funder
Japan Society for the Promotion of Science
Publisher
Elsevier BV
Subject
Issues, ethics and legal aspects,Pathology and Forensic Medicine
Reference27 articles.
1. Inherited ADAMTS13 deficiency (Upshaw-Schulman syndrome): a short review;Pérez-Rodríguez;Thromb. Res.,2014
2. ADAMTS13 activity and genetic mutations in Japan;Miyata;Hämostaseologie,2013
3. Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura;Levy;Nature,2001
4. Structure of von Willebrand factor-cleaving protease (ADAMTS13), a metalloprotease involved in thrombotic thrombocytopenic purpura;Zheng;J. Biol. Chem.,2001
5. A novel human metalloprotease synthesized in the liver and secreted into the blood: possibly, the von Willebrand factor-cleaving protease?;Soejima;J. Biochem.,2001
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