Genomics of bleeding disorders-Reference-Cited by-同舟云学术

Genomics of bleeding disorders

Published:2014-04-25 Issue: Volume:20 Page:50-53
ISSN:1351-8216
Container-title:Haemophilia
language:en
Short-container-title:Haemophilia

Author:

Goodeve A. C.¹,Pavlova A.²,Oldenburg J.²

Affiliation:

1. Sheffield Diagnostic Genetics Service; Sheffield Children's NHS Foundation Trust and Haemostasis Research Group; Department of Cardiovascular Science; University of Sheffield; Sheffield UK

2. Institute of Experimental Haematology and Transfusion Medicine; University Clinic Bonn; Bonn Germany

Publisher

Wiley

Subject

Genetics(clinical),Hematology,General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/hae.12424/fullpdf

Reference31 articles.

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2. Combined deficiency of factor V and factor VIII is due to mutations in either LMAN1 or MCFD2;Zhang;Blood,2006

3. Mutations in VKORC1 cause warfarin resistance and multiple coagulation factor deficiency type 2;Rost;Nature,2004

4. Severe hemophilia with mild bleeding phenotype: molecular characterization and global coagulation profile;Santagostino;J Thromb Haemost,2010

5. Correlation between phenotype and genotype in a large unselected cohort of children with severe hemophilia A;Carcao;Blood,2013

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