SLFN14-related thrombocytopenia: identification within a large series of patients with inherited thrombocytopenia-Reference-Cited by-同舟云学术

SLFN14-related thrombocytopenia: identification within a large series of patients with inherited thrombocytopenia

Published:2016 Issue:05 Volume:115 Page:1076-1079
ISSN:0340-6245
Container-title:Thrombosis and Haemostasis
language:en
Short-container-title:Thromb Haemost

Author:

Marconi Caterina,Di Buduo Christian A.,Barozzi Serena,Palombo Flavia,Pardini Simonetta,Zaninetti Carlo,Pippucci Tommaso,Noris Patrizia,Balduini Alessandra,Seri Marco,Pecci Alessandro

Abstract

Supplementary Material to this article is available online at www.thrombosis-online.com.

Funder

Telethon Foundation

Cariplo Foundation

Publisher

Georg Thieme Verlag KG

Subject

Hematology

Link

http://www.thieme-connect.de/products/ejournals/pdf/10.1160/TH15-11-0884.pdf

Reference15 articles.

1. Pecci A. Diagnosis and treatment of inherited thrombocytopenias. Clin Genet 2015; Epub ahead of print

2. Progress in understanding the diagnosis and molecular genetics of macrothrombocytopenias

3. Deleterious mutation in the FYB gene is associated with congenital autosomal recessive small-platelet thrombocytopenia

5. SLFN14 mutations underlie thrombocytopenia with excessive bleeding and platelet secretion defects

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