T. Bird

APP717, APP693, and PRIP gene mutations are rare in Alzheimer disease.

G. Schellenberg, W. Kukull, M. Ball, 1991, American journal of human genetics.

A novel progranulin mutation associated with variable clinical presentation and tau, TDP43 and alpha-synuclein pathology.

G. Schellenberg, T. Montine, V. Lee, 2007, Brain : a journal of neurology.

β-Synuclein gene alterations in dementia with Lewy bodies

J. Trojanowski, V. Lee, A. Kakita, 2004, Neurology.