Spataro et al., 2019 - Mutations in ATP13A2 (PARK9) are associated with an amyotrophic lateral sclerosis-like phenotype, implicating this locus in further phenotypic expansion. Human genomics   13:19 Full text @ Hum. Genomics
Human Disease / Model Data (1 Record)
Human Disease Fish Environment Evidence Code
amyotrophic lateral sclerosis WT + MO2-atp13a2 + MO3-atp13a2 standard conditions
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