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Rare variants in GP1BB are responsible for autosomal dominant macrothrombocytopenia. (2017)

First Author: Sivapalaratnam S

Attributed to: Modernising the diagnosis of mucocutaneous bleeding disorders: next generation sequencing of novel loci associated with platelet dysfunction. 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