| Literature DB >> 24335028 |
Abstract
In this issue of Blood, Stockley et al describe mutations in FLI1 and RUNX1, identified by next-generation sequencing (NGS) studies, in 6 of 13 patients with excessive bleeding and impaired platelet dense granule secretion, and highlight transcription factor (TF) mutations as an important mechanism for inherited platelet dysfunction.Entities:
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Year: 2013 PMID： 24335028 DOI： 10.1182/blood-2013-10-533166
Source DB: PubMed Journal: Blood ISSN： 0006-4971 Impact factor: 22.113