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

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

https://www.repository.cam.ac.uk/handle/1810/297860

Repository DOI

https://doi.org/10.17863/CAM.44917

Files

Accepted version (1.91 MB)

Type

Authors

Meijers, Joost CM

Huntington, James A

Mulder, André B

Keywords

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

Journal Title

Haematologica

Journal ISSN

0390-6078
1592-8721

Volume Title

105

Publisher

Ferrata Storti Foundation (Haematologica)

Publisher DOI

https://doi.org/10.3324/haematol.2019.232504

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