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Article

ATP1A3 mutation in the first asian case of rapid-onset dystonia-parkinsonism.

Movement disorders : official journal of the Movement Disorder Society - 15 Sept 2007

Lee Jee-Young, Gollamudi Seema, Ozelius Laurie J, Kim Ji-Young, Jeon Beom S

Abstract excerpt

We report a 38-year-old Korean man with sporadic rapid-onset dystonia-parkinsonism (RDP), who had a Thr 618 Met mutation in the Na(+)/K(+)-ATPase alpha3 subunit gene (ATP1A3). At the age of 21, he acutely developed severe dystonia and parkinsonism, which rapidly deteriorated into a wheelchair-bou...

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Identifiers

PMID: 17595045
DOI: 10.1002/mds.21638

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-17595045-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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