Fig. 2From: Mutations in ATP13A2 (PARK9) are associated with an amyotrophic lateral sclerosis-like phenotype, implicating this locus in further phenotypic expansionSchematic of ATP13A2 showing the hydrolase, as well as the P5- and E1-E2-ATPase protein domains. The mutations described in this study to be associated with an ALS-like phenotype are shown in black font. The variants in patients with Kufor-Rakeb syndrome are shown in blue, and the changes associated with hereditary spastic paraplegia are shown in magentaBack to article page