Afibrinogenemia with two compound heterozygous mutations in FGA gene-Reference-Cited by-同舟云学术

Afibrinogenemia with two compound heterozygous mutations in FGA gene

Published:2021-07-13 Issue:5 Volume:27 Page:
ISSN:1351-8216
Container-title:Haemophilia
language:en
Short-container-title:Haemophilia

Author:

Feugray Guillaume¹,Billoir Paul¹^ORCID,Casini Alessandro²^ORCID,Neerman‐Arbez M.³^ORCID,Barbay Virginie¹⁴,Chamouni Pierre⁴,Schneider Pascale⁵,Le Cam Duchez Véronique¹⁴

Affiliation:

1. UNIROUEN INSERM U1096 Vascular Hemostasis Unit Normandie University, Rouen University Hospital France

2. Division of Angiology and Hemostasis Faculty of Medicine Geneva University Hospitals Geneva Switzerland

3. Department of Genetic Medicine and Development Faculty of Medicine University of Geneva Geneva Switzerland

4. Hemophilia Care Center Rouen University Hospital Rouen France

5. Department of Pediatric Hematology and Oncology Rouen University Hospital Rouen France

Publisher

Wiley

Subject

Genetics(clinical),Hematology,General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/hae.14377

Reference10 articles.

1. Congenital Fibrinogen Disorders: An Update

2. Rare bleeding disorders: diagnosis and treatment

3. Clinical phenotype, fibrinogen supplementation, and health-related quality of life in patients with afibrinogenemia

4. Comparison of markers of coagulation activation and thrombin generation test in uncomplicated pregnancies

5. Fibrinogen Fractions in the Third Trimester of Pregnancy and in Puerperium

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