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UnknownFactors in the disease severity of ATP1A3 mutations: Impairment, misfolding, and allele competition.
Not available
S-EPMC7397496 | biostudies-literature
UnknownA dystonia-like movement disorder with brain and spinal neuronal defects is caused by mutation of the mouse laminin β1 subunit, Lamb1.
Not available
S-EPMC4749547 | biostudies-literature
UnknownRapid-Onset Dystonia-Parkinsonism Phenotype Consistency for a Novel Variant of ATP1A3 in Patients Across 3 Global Populations.
Not available
S-EPMC8105889 | biostudies-literature
UnknownIn vivo prime editing rescues alternating hemiplegia of childhood in mice.
Not available
S-EPMC12702498 | biostudies-literature
UnknownAlternating hemiplegia of childhood associated mutations in Atp1a3 reveal diverse neurological alterations in mice.
Not available
S-EPMC12798733 | biostudies-literature
UnknownDe novo ATP1A3 and compound heterozygous NLRP3 mutations in a child with autism spectrum disorder, episodic fatigue and somnolence, and muckle-wells syndrome.
Not available
S-EPMC6005789 | biostudies-literature
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