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.
Haematologica. 2019 Oct 03;:
Authors: Mulder R, Lisman T, Meijers JCM, Huntington JA, Mulder AB, Meijer K
Abstract
PMID: 31582550 [PubMed - as supplied by publisher]
Source: Haematologica - Category: Hematology Authors: Mulder R, Lisman T, Meijers JCM, Huntington JA, Mulder AB, Meijer K Tags: Haematologica Source Type: research