Alpha-synuclein null mutation exacerbates the phenotype of a model of Menkes disease in female mice
MegAnne Casey, Dan Zou, Renee A. Reijo Pera, Tiffany Hensley‐McBain, Deborah E. Cabin
This study identifies Snca as a genetic modifier of Atp7a in female mice, revealing a potential role for Snca in the ER-Golgi system in a sex-dependent manner.
Frontiers in Neuroscience · Jul 3, 2025Peer-reviewedNeuroscience