| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 8679281 | Thrombosis Research | 2018 | 24 Pages |
Abstract
Targeted NGS identified a common indel variant rs8176719 in the ABO gene. Gene-based tests of association failed to reveal genomic loci with a cumulative burden of rare variants associated with CVT.
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Authors
Marcin M. Gorski, Hugoline G. de Haan, Ilaria Mancini, Luca A. Lotta, Paolo Bucciarelli, Serena M. Passamonti, Andrea Cairo, Emanuela Pappalardo, Astrid van Hylckama Vlieg, Ida Martinelli, Frits R. Rosendaal, Flora Peyvandi,