Prothrombotic variants as modifiers of clinical phenotype in four related individuals with haemophilia A-Reference-Cited by-同舟云学术

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Prothrombotic variants as modifiers of clinical phenotype in four related individuals with haemophilia A

Published:2021-05-29 Issue:4 Volume:27 Page:
ISSN:1351-8216
Container-title:Haemophilia
language:en
Short-container-title:Haemophilia

Author:

Carrel Laura¹^ORCID,Arnold‐Croop Sarah²,Achtermann Ty²,Chen Fang³,Cheng Yuhuan³,Liu Dajiang³,Eyster M. Elaine²

Affiliation:

1. Department of Biochemistry and Molecular Biology Penn State College of Medicine Hershey PA USA

2. Division of Hematology and Oncology Department of Medicine Penn State Health Milton S. Hershey Medical Center Hershey PA USA

3. Department of Public Health Sciences Penn State College of Medicine Hershey PA USA

Publisher

Wiley

Subject

Genetics(clinical),Hematology,General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/hae.14348

Reference15 articles.

1. Variation in baseline factorVIIIconcentration in a retrospective cohort of mild/moderate hemophilia A patients carrying identicalF8mutations

2. Modifiers of clinical phenotype in severe congenital hemophilia

3. Identified unmet needs and proposed solutions in mild‐to‐moderate haemophilia: A summary of opinions from a roundtable of haemophilia experts

4. The pennsylvania hemophilia program 1973–1978

5. The European Association for Haemophilia and Allied Disorders (EAHAD) Coagulation Factor Variant Databases: Important resources for haemostasis clinicians and researchers

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