E. Hayman

Changing patterns of bleeding in patients with severe haemophilia A

G. Dolan, D. Stephensen, G. Dolan, 2009, Haemophilia : the official journal of the World Federation of Hemophilia.

Severe factor X deficiency due to a homozygous mutation (Cys364Arg) that disrupts a disulphide bond in the catalytic domain

D. Perry, T. Baglin, M. Gattens, 2006, Haemophilia : the official journal of the World Federation of Hemophilia.

B56δ-related protein phosphatase 2A dysfunction identified in patients with intellectual disability.

M. Hurles, L. Vissers, A. Hoischen, 2015, The Journal of clinical investigation.