Defective acid hydrolase secretion inRUNX1haplodeficiency: Evidence for a global platelet secretory defect-Reference-Cited by-同舟云学术

Defective acid hydrolase secretion inRUNX1haplodeficiency: Evidence for a global platelet secretory defect

Published:2017-06-29 Issue:5 Volume:23 Page:784-792
ISSN:1351-8216
Container-title:Haemophilia
language:en
Short-container-title:Haemophilia

Author:

Rao A. K.¹^ORCID,Poncz M.²

Affiliation:

1. Sol Sherry Thrombosis Research Center and the Hematology Division; Department of Medicine; Lewis Katz School of Medicine at Temple University; Philadelphia PA USA

2. Hematology Division; Children's Hospital of Philadelphia; Philadelphia PA USA

Funder

National Institutes of Health

Publisher

Wiley

Subject

Genetics (clinical),Hematology,General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/hae.13280/fullpdf

Reference28 articles.

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4. In vitro analyses of known and novel RUNX1/AML1 mutations in dominant familial platelet disorder with predisposition to acute myelogenous leukemia: implications for mechanisms of pathogenesis;Michaud;Blood,2002

5. Inherited platelet function disorders: overview and disorders of granules, secretion, and signal transduction;Rao;Hematol Oncol Clin North Am,2013

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