Your search returned 128 results.

Sort
Results
101.
102.
103.
104.
105.
106.
107.
108.
109.
110.
111.
112.
113.
114.
115.
116.
117.
The CALHM1 P86L polymorphism is a genetic modifier of age at onset in Alzheimer's disease: a meta-analysis study. [electronic resource] by
Producer: 20110829 In: Journal of Alzheimer's disease : JAD vol. 22
Availability: No items available.

118.
119.
Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration. [electronic resource] by
Producer: 20150608 In: Acta neuropathologica vol. 128
Availability: No items available.

120.
TBK1 Mutation Spectrum in an Extended European Patient Cohort with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis. [electronic resource] by
Producer: 20171222 In: Human mutation vol. 38
Availability: No items available.