Genetic variants at the chromosomal region 2q21.3 underlying inhibitor development in patients with severe haemophilia A-Reference-Cited by-同舟云学术

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Genetic variants at the chromosomal region 2q21.3 underlying inhibitor development in patients with severe haemophilia A

Published:2022-02-19 Issue:2 Volume:28 Page:270-277
ISSN:1351-8216
Container-title:Haemophilia
language:en
Short-container-title:Haemophilia

Author:

Spena Silvia¹,Cairo Andrea¹,Pappalardo Emanuela²,Gorski Marcin M.²,Garagiola Isabella¹,Hassan Shermarke²³,Gualtierotti Roberta¹²,Peyvandi Flora¹²

Affiliation:

1. Angelo Bianchi Bonomi Hemophilia and Thrombosis Center, Fondazione IRCCS Ca’ Granda Ospedale Maggiore Policlinico, and Luigi Villa Foundation Milan Italy

2. Department of Pathophysiology and Transplantation Università degli Studi di Milano Milan Italy

3. Department of Clinical Epidemiology Leiden University Medical Center Leiden the Netherlands

Publisher

Wiley

Subject

Genetics (clinical),Hematology,General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/hae.14503

Reference37 articles.

1. The Hemophilias — From Royal Genes to Gene Therapy

2. The past and future of haemophilia: diagnosis, treatments, and its complications

3. Factor VIII inhibitors in hemophilia A: rationale and latest evidence

4. Factor VIII Inhibitor-Bypassing Agents Act by Inducing Thrombin Generation and Can Be Monitored by a Thrombin Generation Assay

5. Emicizumab, a bispecific antibody recognizing coagulation factors IX and X: how does it actually compare to factor VIII?

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