Genomic approaches to bleeding disorders-Reference-Cited by-同舟云学术

Genomic approaches to bleeding disorders

Published:2016-07 Issue: Volume:22 Page:42-45
ISSN:1351-8216
Container-title:Haemophilia
language:en
Short-container-title:Haemophilia

Author:

Peyvandi F.¹²,Hayward C. P. M.³

Affiliation:

1. Angelo Bianchi Bonomi Hemophilia and Thrombosis Center; Fondazione IRCCS Ca’ Granda Ospedale Maggiore Policlinico; Milan Italy

2. Department of Pathophysiology and Transplantation; Università degli Studi di Milano; Milan Italy

3. Department of Pathology and Molecular Medicine; McMaster University; Hamilton ON Canada

Funder

Bayer

Biotest

CSL Behring

Grifols

Novo Nordisk

Sobi

Alexion Pharmaceuticals

Kedrion Biopharma

Fondazione Luigi Villa

Publisher

Wiley

Subject

Genetics(clinical),Hematology,General Medicine

Reference24 articles.

1. Inversions disrupting the factor VIII gene are a common cause of severe haemophilia A;Lakich;Nat Genet,1993

2. Recurrent inversion breaking intron 1 of the factor VIII gene is a frequent cause of severe haemophilia A;Bagnall;Blood,2002

3. Zivelin A Seligsohn U Deficiencies of prothrombin, factor V, factor VII, factor X, factor XI, factor XIII, combined factors V and VIII, and vitamin K dependent coagulation factors http://www.isth.org/?MutationsRareBleedin

4. Introduction. Rare bleeding disorders: general aspects of clinical features, diagnosis, and management;Peyvandi;Semin Thromb Hemost,2009

5. Exome sequencing identifies the cause of a mendelian disorder;Ng;Nat Genet,2010

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