A rare cause of bleeding in two Indian families with congenital alpha‐2‐antiplasmin deficiency-Reference-Cited by-同舟云学术

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A rare cause of bleeding in two Indian families with congenital alpha‐2‐antiplasmin deficiency

Published:2019-10-02 Issue:6 Volume:25 Page:
ISSN:1351-8216
Container-title:Haemophilia
language:en
Short-container-title:Haemophilia

Author:

Prabhudesai Aniket¹,Shetty Shrimati¹^ORCID,Shanmukhaiah Chandrakala²,Kalantri Siddhesh³^ORCID,Bhattacharyya Maitreyee³^ORCID,Kulkarni Bipin¹^ORCID

Affiliation:

1. Department of Thrombosis and Haemostasis National Institute of Immunohaematology (ICMR)KEM Hospital Campus Mumbai India

2. Department of Haematology Seth GS Medical College and KEM Hospital Mumbai India

3. Institute of Hematology and Transfusion Medicine Medical College and Hospital Kolkata Kolkata India

Publisher

Wiley

Subject

Genetics(clinical),Hematology,General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/hae.13851

Reference8 articles.

1. Effects of α2-Plasmin Inhibitor on Fibrin Clot Lysis. Its Comparison with α2-Macroglobulin

2. Congenital α2-plasmin inhibitor deficiencies: a review

3. A new euglobulin clot lysis assay for global fibrinolysis

4. α2-PLASMIN-INHIBITOR DEFICIENCY (MIYASATO DISEASE)

5. A novel allele variant of the SERPINF2 gene responsible for severe plasmin inhibitor (α 2 -antiplasmin) deficiency in an Italian patient

Cited by 1 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. Congenital Alpha-2 Antiplasmin Deficiency: a Literature Survey and Analysis of 123 Cases;Clinical Laboratory;2020

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