Filters: Author is Klein, Eric [Clear All Filters]
Mutations in rare ataxia genes are uncommon causes of sporadic cerebellar ataxia.. Movement disorders : official journal of the Movement Disorder Society. 27(3):442-6.. 2012.
Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseases.. Human molecular genetics. 21(15):3500-12.. 2012.