Phenotype analysis and clinical management in a large family with a novel truncating mutation inRASGRP2, the CalDAG-GEFI encoding gene-Reference-Cited by-同舟云学术

Phenotype analysis and clinical management in a large family with a novel truncating mutation inRASGRP2, the CalDAG-GEFI encoding gene

Published:2017-06-20 Issue:1 Volume:1 Page:128-133
ISSN:2475-0379
Container-title:Research and Practice in Thrombosis and Haemostasis
language:en
Short-container-title:Res Pract Thromb Haemost

Author:

Desai Amrita¹,Bergmeier Wolfgang²,Canault Mathias³,Alessi Marie-Christine³,Paul David S.²,Nurden Paquita⁴,Pillois Xavier⁴,Jy Wenche¹,Ahn Yeon S.¹,Nurden Alan T.⁴

Affiliation:

1. Division of Hematology/Oncology; University of Miami; Miami FL USA

2. McAllister Heart Institute and Department of Biochemistry and Biophysics; University of North Carolina at Chapel Hill; Chapel Hill NC USA

3. Aix Marseille Univ; INSERM; INRA; Marseille France

4. IHU-LIRYC; Plateforme Technologique D'Innovation Biomédicale Hopital Xavier Arnozan; Pessac France

Funder

National Heart, Lung, and Blood Institute

Publisher

Wiley

Subject

Hematology

Reference22 articles.

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4. The final steps of integrin activation: the end game;Shattil;Nat Rev Mol Cell Biol,2010

5. CalDAG-GEFI and protein kinase C represent alternative pathways leading to activation of integrin alphaIIbbeta3 in platelets;Cifuni;Blood,2008

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