Clinical, biological, and genetic features in an afibrinogenemia patient series in Algeria-Reference-Cited by-同舟云学术

Clinical, biological, and genetic features in an afibrinogenemia patient series in Algeria

Published:2022-04-30 Issue:5 Volume:28 Page:822-831
ISSN:1351-8216
Container-title:Haemophilia
language:en
Short-container-title:Haemophilia

Author:

Hadjali‐Saichi Soraya¹,de Mazancourt Philippe²^ORCID,Tapon‐Bretaudière Jacqueline³,Mirault Tristan⁴,Guenounou Kahina¹,Frigaa Issam¹,Fischer Anne‐Marie³,Chafa Ouerdia¹,Helley Dominique³

Affiliation:

1. Center for Hemobiology‐Blood Transfusion Mustapha University Hospital Faculty of Medicine of Algiers Algiers Algeria

2. Laboratory of molecular biology and UVSQ UMR 1179 Ambroise Paré Hospital Boulogne‐Billancourt France

3. Hematology department European Georges Pompidou Hospital Paris University, and UMR‐S 970 Paris France

4. Vascular Medicine department European Georges Pompidou Hospital Paris France

Publisher

Wiley

Subject

Genetics (clinical),Hematology,General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/hae.14579

Reference35 articles.

1. Fibrin Formation, Structure and Properties

2. Missense mutations in the human β fibrinogen gene cause congenital afibrinogenemia by impairing fibrinogen secretion

3. Congenital Fibrinogen Disorders

4. Bleeding and thrombosis in 55 patients with inherited afibrinogenaemia

5. Rare Coagulation Disorders

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