Eye movement disorders in ATP13A2 mutation carriers (PARK9)

Movement Disorders

Volumn 25, Issue 15, 2010, Pages 2687-2689

  Machner, Björn ^a   Sprenger, Andreas ^a   Behrens, Maria Isabel ^b   Ramirez, Alfredo ^a   Brüggemann, Norbert ^a   Klein, Christine ^a   Helmchen, Christoph ^a,b  

^a UNIVERSITY OF LÜBECK   (Germany)

^b HOSPITAL CLÍNICO UNIVERSIDAD DE CHILE   (Chile)

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE TRIPHOSPHATASE; ATP13A2 PROTEIN; UNCLASSIFIED DRUG;

ADULT; AGED; CHILE; CLINICAL ARTICLE; CONTROLLED STUDY; EXTRAPYRAMIDAL SYMPTOM; EYE MOVEMENT DISORDER; GENE MUTATION; HETEROZYGOTE; HUMAN; KUFOR RAKEB DISEASE; LETTER; OPTOKINETIC NYSTAGMUS; PARKINSONISM; PATHOPHYSIOLOGY; PRIORITY JOURNAL; SACCADIC EYE MOVEMENT; UNIFIED PARKINSON DISEASE RATING SCALE;

ADULT; AGED; CHILE; EYE MOVEMENT MEASUREMENTS; EYE MOVEMENTS; FEMALE; HETEROZYGOTE; HUMANS; MALE; MIDDLE AGED; MUTATION; OCULAR MOTILITY DISORDERS; PROTON-TRANSLOCATING ATPASES;

EID: 78349233855     PISSN: 08853185     EISSN: 15318257     Source Type: Journal    
DOI: 10.1002/mds.23352     Document Type: Letter

References (7)

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3. Behrens MI, Brüggemann N, Chana P, et al. Clinical spectrum of Kufor Rakeb syndrome in the Chilean kindred with ATP13A2 mutations. Mov Disord (in press).
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