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Paper Details

De novo mutations in ATP1A3 cause alternating hemiplegia of childhood.
Nat Genet
292
2012
AHC, ATP1A3, ATP1A3 mutations, ATPase, Alternating hemiplegia of childhood, alternating hemiplegia of childhood, dystonia-parkinsonism, familial AHC, hemiplegic episodes, neurodevelopmental syndrome, patients
Author NameAffiliation
Erin L HeinzenCenter for Human Genome Variation, Duke University School of Medicine
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Release 1.2