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
Repository URI
Repository DOI
Change log
Authors
Description
Keywords
Genetic Linkage, Humans, Mutation, Pedigree, Prothrombin, Thrombosis, Exome Sequencing
Journal Title
Haematologica
Conference Name
Journal ISSN
0390-6078
1592-8721
1592-8721
Volume Title
105
Publisher
Ferrata Storti Foundation (Haematologica)
Publisher DOI
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All rights reserved