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A dominant gain-of-function mutation in universal tyrosine kinase SRC causes thrombocytopenia, myelofibrosis, bleeding, and bone pathologies. (2016)

First Author: Turro E

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/10.1126/scitranslmed.aad7666

PubMed Identifier: 26936507

Publication URI: http://europepmc.org/abstract/MED/26936507

Type: Journal Article/Review

Volume: 8

Parent Publication: Science translational medicine

Issue: 328

ISSN: 1946-6234