G. Tennent

Human lysozyme gene mutations cause hereditary systemic amyloidosis

D. Booth, C. Blake, M. Pepys, 1993, Nature.

Disease‐associated prion protein is not detectable in human systemic amyloid deposits

M. Pepys, P. Hawkins, G. Tennent, 2007, The Journal of pathology.

Transthyretin Ile84Thr is associated with familial amyloid polyneuropathy

P. Hawkins, J. Gillmore, A. Stangou, 2000, Human mutation.

Molecular mechanisms of fibrillogenesis and the protective role of amyloid P component: two possible avenues for therapy.

S. Radford, D. Booth, C. Robinson, 1996, Ciba Foundation symposium.