Exome sequencing identifies GATA-2 mutation as the cause of dendritic cell, monocyte, B and NK lymphoid deficiency
Rachel Dickinson, Matthew Collin(Newcastle upon Tyne Hospitals NHS Foundation Trust), Patrick F. Chinnery(Wellcome Centre for Mitochondrial Research), John Loughlin(Freeman Hospital), David McDonald, Louise N. Reynard, Sharon Cookson, Naomi McGovern, Sophie Hambleton(Newcastle upon Tyne Hospitals NHS Foundation Trust), Bernard Keavney(Manchester Academic Health Science Centre), Sarah Pagan, Jeremy H. Lakey(Newcastle University), Helen Griffin(NIHR Newcastle Biomedical Research Centre), Mauro Santibanez‐Koref(Newcastle University), Venetia Bigley(National Health Service), Muzlifah Haniffa(Wellcome Sanger Institute), Rafiqul Hussain(Centre for Life), Xiao-Nong Wang, Jonathan P. Wallis(National Health Service), Andrew J. Cant(Clinical Research Institute), Ignatius Chua(The Royal Free Hospital), Thahira Rahman(Centre for Life), Michael Wright(Newcastle upon Tyne Hospital)
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