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