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Linkage analysis combined with whole-exome sequencing identifies a novel prothrombin (F2) gene mutation in a Dutch Caucasian family with unexplained thrombosis.

Accepted version
Peer-reviewed

Type

Article

Change log

Authors

Mulder, René 
Lisman, Ton 
Meijers, Joost CM 
Huntington, James A 
Mulder, André B 

Description

Keywords

Genetic Linkage, Humans, Mutation, Pedigree, Prothrombin, Thrombosis, Exome Sequencing

Journal Title

Haematologica

Conference Name

Journal ISSN

0390-6078
1592-8721

Volume Title

105

Publisher

Ferrata Storti Foundation (Haematologica)

Rights

All rights reserved