Rare variants in GP1BB are responsible for autosomal dominant macrothrombocytopenia. (2017)
Attributed to:
Large-scale integrative studies of risk factors in coronary heart disease: from discovery to application
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1182/blood-2016-08-732248
PubMed Identifier: 28064200
Publication URI: http://europepmc.org/abstract/MED/28064200
Type: Journal Article/Review
Volume: 129
Parent Publication: Blood
Issue: 4
ISSN: 0006-4971