Molecular bases of antithrombin deficiency: twenty-two novel mutations in the antithrombin gene-Reference-Cited by-同舟云学术

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Molecular bases of antithrombin deficiency: twenty-two novel mutations in the antithrombin gene

Published:2006 Issue:6 Volume:27 Page:600-600
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Picard Véronique,Nowak-Göttl Ulrike,Biron-Andreani Christine,Fouassier Marc,Frere Corinne,Goualt-Heilman Michèle,de Maistre Emmanuel,Regina Sandra,Rugeri Lucia,Ternisien Catherine,Trichet Catherine,Vergnes Christine,Aiach Martine,Alhenc-Gelas Martine

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Cited by 51 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. Clinical and functional characterization of rare compound heterozygous mutations in the SERPINC1 gene causing severe thrombophilia;Gene;2024-03

2. Multiple venous thromboembolisms in a pregnant patient carrying a novel mutation in SERPINC1 (p.M313T) that causes a transient antithrombin deficiency: a case report;Thrombosis Journal;2023-12-13

3. Antithrombin III activity is associated with prognosis, infection, and inflammation in patients with hepatitis B virus-related acute-on-chronic liver failure;European Journal of Gastroenterology & Hepatology;2023-06-28

4. Antithrombin Deficiency Is Associated with Prothrombotic Plasma Fibrin Clot Phenotype;Thrombosis and Haemostasis;2023-05-18

5. A review of laboratory considerations in thrombophilia testing;Pathology;2022-12

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