Dr Helen GriffinResearch Associate
Email: helen.griffin@ncl.ac.uk Telephone: +44 (0) 191 241 8818 Address: Institute of Human Genetics
Dickinson RE, Griffin H, Bigley V, Reynard LN, Hussain R, Haniffa M, Lakey JH, Rahman T, Wang XN, McGovern N, Pagan S, Cookson S, McDonald D, Chua I, Wallis J, Cant A, Wright M, Keavney B, Chinnery PF, Loughlin J, Hambleton S, Santibanez-Koref M, Collin M. Exome sequencing identifies GATA-2 mutation as the cause of the dendritic cell, monocyte, B and NK lymphoid deficiency .
Blood 2011, 118 (10), 2656-2658.
Dickinson RE, Bigley V, Griffin H, Lakey JH, McGovern N, Chua I, Wallis J, Hambleton S, Santibanez-Koref M, Collin M. Human dendritic cell deficiency is caused by GATA-2 mutation .
In: Immunology: Annual Congress of the British Society for Immunology . 2011, Liverpool, UK: Wiley-Blackwell Publishing Ltd.
McDonald D, Morgan N, Griffin H, Dang TS, Grainger A, Reynard L, Loughlin J, Santibanez-Koref M, Hambleton S. Whole-exome deep sequencing identifies a novel causative mutation in primary immunodeficiency .
In: Immunology: Annual Congress of the British Society for Immunology . 2011, Liverpool, UK: Wiley-Blackwell Publishing Ltd.
