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Further characterization of CAPOS/CAOS syndrome with the Glu818Lys mutation in the ATP1A3 gene: A case report | Semantic Scholar
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Parkinsonism & Related Disorders on Twitter: "#Dystonia #deafness #ATP1A3 # CAPOS Log in to: https://t.co/OaOj1URbYq https://t.co/xQ0wsK7k1g" / Twitter
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Further characterization of CAPOS/CAOS syndrome with the Glu818Lys mutation in the ATP1A3 gene: A case report | Semantic Scholar
Cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss (CAPOS): a new syndrome. - Abstract - Europe PMC
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