The odds and implications of coinheritance of hemophilia A and B-Reference-Cited by-同舟云学术

The odds and implications of coinheritance of hemophilia A and B

Published:2020-07 Issue:5 Volume:4 Page:931-935
ISSN:2475-0379
Container-title:Research and Practice in Thrombosis and Haemostasis
language:en
Short-container-title:Res Pract Thromb Haemost

Author:

Karch Corinne¹,Masser‐Frye Diane²,Limjoco Jacqueline²,Ryan Sarah E.³,Fletcher Shelley N.³,Corbett Kevin D.⁴^ORCID,Johnsen Jill M.³⁵^ORCID,Thornburg Courtney D.²⁶^ORCID

Affiliation:

1. Virginia Commonwealth University School of Medicine Richmond Virginia USA

2. Rady Children’s Hospital San Diego San Diego California USA

3. Bloodworks Northwest Seattle Washington USA

4. Department of Cellular and Molecular Medicine University of California San Diego La Jolla California USA

5. Department of Medicine University of Washington Seattle Washington USA

6. Department of Pediatrics University of California San Diego La Jolla California USA

Publisher

Wiley

Subject

Hematology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/rth2.12345

Reference20 articles.

1. Genetic diagnosis in hemophilia and von Willebrand disease

2. Combined factor VIII and IX deficiency in a family

3. A de novo factor VIII mutation in a haemophilia B family leading to combined deficiency of factor VIII and IX

4. F8 and F9 mutations fail to co-segregate in a family with co-incident haemophilia A and B

5. Combined coagulation factor VIII and factor IX deficiency (CDF8F9) in a patient from Lithuania;Ivaskevicius V;Hamostaseologie,2016

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