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Genomic approaches to bleeding disorders
Conference

Genomic approaches to bleeding disorders

Abstract

The genes encoding the coagulation factors were characterized over two decades ago. Since then, significant progress has been made in the genetic diagnosis of the two commonest severe inherited bleeding disorders, haemophilia A and B. Experience with the genetic of inherited rare bleeding disorders and platelet disorders is less well advanced. Rare bleeding disorders are usually inherited as autosomal recessive disorders, while it is now clear …

Authors

Peyvandi F; Hayward CPM

Volume

22

Pagination

pp. 42-45

Publisher

Wiley

Publication Date

July 2016

DOI

10.1111/hae.12998

Conference proceedings

Haemophilia

Issue

S5

ISSN

1351-8216