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Long-Term Follow-Up of a Patient with a De Novo p.Arg769Cys Mutation in the ATP1A3 Gene
Long-Term Follow-Up of a Patient with a De Novo p.Arg769Cys Mutation in the ATP1A3 Gene
2021
Anjali Chouksey
Asish Vijayaraghavan
Sony Mohan
Srija Inturi
A. T. Prabhakar
Vivek Mathew
Keywords:
CAPOS syndrome
Alternating hemiplegia of childhood
Gene
ATP1A3
Rapid-Onset Dystonia Parkinsonism
long term follow up
Mutation (genetic algorithm)
Pediatrics
Medicine
Correction
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