Megakaryocytic emperipolesis and platelet function abnormalities in five patients with gray platelet syndrome-Reference-Cited by-同舟云学术

Megakaryocytic emperipolesis and platelet function abnormalities in five patients with gray platelet syndrome

Published:2015-03-25 Issue:8 Volume:26 Page:751-757
ISSN:0953-7104
Container-title:Platelets
language:en
Short-container-title:Platelets

Author:

Larocca Luigi M.,Heller Paula G.,Podda Gianmarco,Pujol-Moix Nuria,Glembotsky Ana C.,Pecci Alessandro,Alberelli Maria Adele,Balduini Carlo L.,Landolfi Raffaele,Cattaneo Marco,De Candia Erica

Publisher

Informa UK Limited

Subject

Hematology,General Medicine

Link

http://www.tandfonline.com/doi/pdf/10.3109/09537104.2014.994093

Reference37 articles.

1. Gray platelet syndrome

2. Mutations in NBEAL2, encoding a BEACH protein, cause gray platelet syndrome

3. NBEAL2 is mutated in gray platelet syndrome and is required for biogenesis of platelet α-granules

4. Exome sequencing identifies NBEAL2 as the causative gene for gray platelet syndrome

5. Correlation between platelet phenotype and NBEAL2 genotype in patients with congenital thrombocytopenia and -granule deficiency

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