Alpha-synuclein null mutation exacerbates the phenotype of a model of Menkes disease in female mice.
MegAnne CaseyDan ZouRenee A Reijo PeraDeborah E CabinPublished in: bioRxiv : the preprint server for biology (2023)
, encodes a copper transporter that is known to act in the trans-Golgi sub-cellular compartment. Genetic modifier effects suggest that Snca may also play a role in that compartment, potentially in the mammalian brain.