Compound heterozygosity involving Antithrombin Cambridge II (p.Ala416Ser) in antithrombin deficiency-Reference-Cited by-同舟云学术

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Compound heterozygosity involving Antithrombin Cambridge II (p.Ala416Ser) in antithrombin deficiency

Published:2013 Issue:03 Volume:109 Page:556-558
ISSN:0340-6245
Container-title:Thrombosis and Haemostasis
language:en
Short-container-title:Thromb Haemost

Author:

Águila Sonia,Martínez-Martínez Irene,Collado Miriam,Llamas Pilar,Antón Ana,Martínez-Redondo Consuelo,Padilla José,Miñano Antonia,de la MorenaBarrio María,García-Avello Ángel,Vicente Vicente,Corral Javier

Funder

Ministerio de Ciencia y Tecnología

Publisher

Georg Thieme Verlag KG

Subject

Hematology

Link

http://www.thieme-connect.de/products/ejournals/pdf/10.1160/TH12-09-0707.pdf

Reference19 articles.

1. Antithrombin Mutation Database: 2nd (1997) Update

2. Amelioration of the severity of heparin-binding antithrombin mutations by posttranslational mosaicism

3. Antithrombin Cambridge II (A384S): an underestimated genetic risk factor for venous thrombosis

4. Heparin-induced substrate behavior of antithrombin Cambridge II

5. Relation between the antithrombin Cambridge II mutation, the risk of venous thrombosis, and the endogenous thrombin generation

Cited by 2 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. β-Antithrombin, subtype of antithrombin deficiency and the risk of venous thromboembolism in hereditary antithrombin deficiency: A family cohort study;Thrombosis Research;2018-08

2. Identification of Regulatory Mutations in SERPINC1 Affecting Vitamin D Response Elements Associated with Antithrombin Deficiency;PLOS ONE;2016-03-22

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