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

Movement Disorders

Volumn 22, Issue 12, 2007, Pages 1808-1809

  Lee, Jee Young ^a,b   Gollamudi, Seema ^c   Ozelius, Laurie J ^c   Kim, Ji Young ^a,b   Jeon, Beom S ^a,b  

^a Seoul National University Hospital   (South Korea)

^b Seoul National University   (South Korea)

^c ALBERT EINSTEIN COLLEGE OF MEDICINE   (United States)

Author keywords

Asian; ATP1A3; Point mutation; Rapid onset dystonia parkinsonism

Indexed keywords

ADENOSINE TRIPHOSPHATASE (POTASSIUM SODIUM); ADENOSINE TRIPHOSPHATASE (POTASSIUM SODIUM) ALPHA3; BACLOFEN; BENSERAZIDE PLUS LEVODOPA; TRIHEXYPHENIDYL; UNCLASSIFIED DRUG;

ADULT; AMINO ACID SUBSTITUTION; ARTICLE; ASIAN; CASE REPORT; DETERIORATION; DISEASE SEVERITY; DYSARTHRIA; DYSPHAGIA; DYSTONIA; ENZYME SUBUNIT; GENE MUTATION; GENETIC SCREENING; HUMAN; KOREA; MALE; MUTATIONAL ANALYSIS; PARKINSONISM; PATIENT MOBILITY; PRIORITY JOURNAL; TREATMENT OUTCOME; WHEELCHAIR;

ADULT; DYSTONIC DISORDERS; HUMANS; KOREA; MALE; METHIONINE; MUTATION; PARKINSONIAN DISORDERS; SODIUM-POTASSIUM-EXCHANGING ATPASE; THREONINE;

EID: 35349007437     PISSN: 08853185     EISSN: 15318257     Source Type: Journal    
DOI: 10.1002/mds.21638     Document Type: Article

References (8)

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