Congenital platelet disorders and understanding of platelet function

Author:

Nurden Alan T.1,Nurden Paquita1

Affiliation:

1. L'Institut de Rhythmologie et Modélisation Cardiaque (LIRYC); Plateforme Technologique et d'Innovation Biomédicale; Hôpital Xavier Arnozan; Pessac France

Publisher

Wiley

Subject

Hematology

Reference103 articles.

1. Inherited human cPLA2α deficiency is associated with impaired eicosanoid biosynthesis, small intestinal ulceration, and platelet dysfunction;Adler;The Journal of Clinical Investigation,2008

2. Munc 18b/STXB2 is required for platelet secretion;Al Hawas;Blood,2012

3. Exome sequencing identifies NBEAL2 as the causative gene for gray platelet syndrome;Albers;Nature Genetics,2011

4. Compound inheritance of a low-frequency regulatory SNP and a rare null mutation in exon-junction complex subunit RBM8A causes TAR syndrome;Albers;Nature Genetics,2012

5. Lentiviral hematopoietic stem cell gene therapy in patients with Wiskott-Aldrich syndrome;Aluti;Science,2013

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