Showing results 1 to 4 of 4
Title | Author(s) | Issue Date | |
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Burden of rare variants in ALS genes influences survival in familial and sporadic ALS Journal:Neurobiology of Aging | 2017 | ||
PMCA4 (ATP2B4) Mutation in Familial Spastic Paraplegia Journal:PLoS ONE | 2014 | ||
PMCA4 (ATP2B4) mutation in familial spastic paraplegia causes delay in intracellular calcium extrusion Journal:Brain and Behavior | 2015 | ||
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