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De novo mutations in ATP1A3 cause alternating hemiplegia of childhood.
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De novo mutations in ATP1A3 cause alternating hemiplegia of childhood.
De novo mutations in ATP1A3 cause alternating hemiplegia of childhood. Nat Genet. 2012 Sep; 44(9):1030-4.
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PubMed
subject areas
Adult
Animals
Child
COS Cells
Family
Female
Genetic Predisposition to Disease
HeLa Cells
Hemiplegia
High-Throughput Nucleotide Sequencing
Humans
Male
Models, Biological
Mutation
Pedigree
Protein Structure, Secondary
Sodium-Potassium-Exchanging ATPase
authors with profiles
Kathryn Swoboda, M.D.