Enhanced inhibitory neurotransmission in the cerebellar cortex of Atp1a3‐deficient heterozygous mice

Key points •  Mutations of ATP1A3 cause rapid‐onset dystonia with parkinsonism (RDP) and alternating hemiplegia of childhood (AHC). •  The mRNA of Atp1a3 was highly expressed in molecular‐layer interneurons and Purkinje cells in the developing mouse cerebellar cortex, and the gene product was observ...

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