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
Morpholino List (2 Records)
Target Reagent
atp13a2 MO2-atp13a2
MO3-atp13a2