Exome sequencing identifies NBEAL2 as the causative gene for gray platelet syndrome
Cornelis A. Albers(Radboud University Nijmegen), Willem H. Ouwehand(NHS Blood and Transplant), Rémi Favier(Inserm), Marie‐Christine Alessi(Inserm), Alan T. Nurden(Hôpital Xavier Arnozan), Paul Bertone(European Bioinformatics Institute), Gregory E. Jordan(Wellcome Trust), Myrto Kostadima(National Health Service), Botond Sipos(Wellcome Trust), Ana Cvejic(University of Copenhagen), Paquita Nurden(Plateforme Technologique d'Innovation Biomédicale), Ross Kettleborough(Wellcome Sanger Institute), Augusto Rendon(University of Cambridge), Katrin Voß(NHS Blood and Transplant), Jonathan Stephens(NHS Blood and Transplant), Randy J. Read(University of Cambridge), Graham Kiddle(University of Cambridge), Peter A. Smethurst(National Health Service), Evelien E. Bouwmans(NHS Blood and Transplant), Suthesh Sivapalaratnam(National Health Service)
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