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
Target | Reagent |
---|---|
atp13a2 | MO2-atp13a2 |
MO3-atp13a2 |