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The Thr224Asn mutation in the VPS45 gene is associated with the congenital neutropenia and primary myelofibrosis of infancy. (2013)

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1182/blood-2012-12-475566

PubMed Identifier: 23599270

Publication URI: http://europepmc.org/abstract/MED/23599270

Type: Journal Article/Review

Volume: 121

Parent Publication: Blood

Issue: 25

ISSN: 0006-4971