Origin of Swedish hemophilia B mutations-Reference-Cited by-同舟云学术

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Origin of Swedish hemophilia B mutations

Published:2013-11 Issue:11 Volume:11 Page:2001-2008
ISSN:1538-7933
Container-title:Journal of Thrombosis and Haemostasis
language:en
Short-container-title:J Thromb Haemost

Author:

Halldén C.¹,Mårtensson A.²,Nilsson D.¹³,Säll T.⁴,Lind-Halldén C.¹,Lidén A. C.¹,Ljung R.²

Affiliation:

1. Biomedicine; Kristianstad University; Kristianstad Sweden

2. Department of Paediatrics and Malmö Centre for Thrombosis and Haemostasis; Skåne University Hospital; Lund University; Malmö Sweden

3. Division of ENT Diseases; Department of Clinical Sciences, Intervention and Technology; Karolinska Institutet; Stockholm Sweden

4. Department of Biology; Lund University; Lund Sweden

Funder

Erik Philip-Sörensens Foundation, Lund University

Region of Skåne

ALF

Regionalt forskningsstöd

The Swedish Research Council

Publisher

Wiley

Subject

Hematology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/jth.12410/fullpdf

Reference15 articles.

1. Deaths in Swedish hemophiliacs, 1957-1980;Larsson;Acta Med Scand,1983

2. Tandem repeats finder: a program to analyze DNA sequences;Benson;Nucleic Acids Res,1999

3. Estimating the age of rare disease mutations: the example of Triple-A syndrome;Genin;J Med Genet,2004

4. Origin of Swedish hemophilia A mutations;Halldén;J Thromb Haemost,2012

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1. Clinical analysis and quality of life survey of hemophilia B patients in the central and western regions of China;Frontiers in Pediatrics;2024-05-09

2. Origin of pathogenic variant and mosaicism in families with a sporadic case of haemophilia B;Haemophilia;2024-04-17

3. Congenital Hemophilia B, Rare Mutation c.368T>G, Presenting with Delayed Massive Expansion of Non-Traumatic Cephalhematoma;Perinatology;2024

4. F8/F9 variants in the population-based PedNet Registry cohort compared with locus-specific genetic databases of the European Association for Haemophilia and Allied Disorders and the Centers for Disease Control and Prevention Hemophilia A or Hemophilia B Mutation Project;Research and Practice in Thrombosis and Haemostasis;2023-01

5. F9 missense mutations impairing factor IX activation are associated with pleiotropic plasma phenotypes;Journal of Thrombosis and Haemostasis;2021-10-24

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