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

Rene Mulder; Ton Lisman; Joost C. M. Meijers; James A. Huntington; Andre B. Mulder; Karina Meijer

doi:10.3324/haematol.2019.232504

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

Rene Mulder^*, Ton Lisman, Joost C. M. Meijers, James A. Huntington, Andre B. Mulder, Karina Meijer

^*Corresponding author for this work

Research output: Contribution to journal › Letter › Academic › peer-review

1 Citation (Scopus)

Original language	English
Pages (from-to)	E370-E372
Number of pages	3
Journal	Haematologica
Volume	105
Issue number	7
DOIs	https://doi.org/10.3324/haematol.2019.232504
Publication status	Published - 1-Jul-2020

Keywords

VENOUS THROMBOEMBOLISM

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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
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@article{6f7460fc7d4440dbb3988ac0feba541b,

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

keywords = "VENOUS THROMBOEMBOLISM",

author = "Rene Mulder and Ton Lisman and Meijers, {Joost C. M.} and Huntington, {James A.} and Mulder, {Andre B.} and Karina Meijer",

year = "2020",

month = jul,

day = "1",

doi = "10.3324/haematol.2019.232504",

language = "English",

volume = "105",

pages = "E370--E372",

journal = "Haematologica",

issn = "0390-6078",

publisher = "FERRATA STORTI FOUNDATION",

number = "7",

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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. / Mulder, Rene; Lisman, Ton; Meijers, Joost C. M.; Huntington, James A.; Mulder, Andre B.; Meijer, Karina.

In: Haematologica, Vol. 105, No. 7, 01.07.2020, p. E370-E372.

Research output: Contribution to journal › Letter › Academic › peer-review

TY - JOUR

T1 - Linkage analysis combined with whole-exome sequencing identifies a novel prothrombin (F2) gene mutation in a Dutch Caucasian family with unexplained thrombosis

AU - Mulder, Rene

AU - Lisman, Ton

AU - Meijers, Joost C. M.

AU - Huntington, James A.

AU - Mulder, Andre B.

AU - Meijer, Karina

PY - 2020/7/1

Y1 - 2020/7/1

KW - VENOUS THROMBOEMBOLISM

U2 - 10.3324/haematol.2019.232504

DO - 10.3324/haematol.2019.232504

M3 - Letter

VL - 105

SP - E370-E372

JO - Haematologica

JF - Haematologica

SN - 0390-6078

IS - 7

ER -