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Fig. 2 | Human Genomics

Fig. 2

From: Mutations in ATP13A2 (PARK9) are associated with an amyotrophic lateral sclerosis-like phenotype, implicating this locus in further phenotypic expansion

Fig. 2

Schematic 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 magenta

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Human Genomics

ISSN: 1479-7364