Eye movement disorders in ATP13A2 mutation carriers (PARK9)
Identifieur interne : 001C93 ( Main/Exploration ); précédent : 001C92; suivant : 001C94Eye movement disorders in ATP13A2 mutation carriers (PARK9)
Auteurs : Björn Machner [Allemagne] ; Andreas Sprenger [Allemagne] ; Maria Isabel Behrens [Chili] ; Alfredo Ramirez [Allemagne] ; Norbert Brüggemann [Allemagne] ; Christine Klein [Allemagne] ; Christoph Helmchen [Allemagne]Source :
- Movement Disorders [ 0885-3185 ] ; 2010-11-15.
Descripteurs français
- Pascal (Inist)
- Wicri :
- geographic : Chili.
English descriptors
- KwdEn :
- MESH :
- chemical , genetics : Proton-Translocating ATPases.
- geographic : Chile.
- genetics : Eye Movements, Ocular Motility Disorders.
- Adult, Aged, Eye Movement Measurements, Female, Heterozygote, Humans, Male, Middle Aged, Mutation.
Url:
DOI: 10.1002/mds.23352
Affiliations:
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Le document en format XML
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<term>Chile</term>
<term>Eye Movement Measurements</term>
<term>Eye Movements (genetics)</term>
<term>Eye movement</term>
<term>Female</term>
<term>Heterozygote</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Mutation</term>
<term>Nervous system diseases</term>
<term>Ocular Motility Disorders (genetics)</term>
<term>Proton-Translocating ATPases (genetics)</term>
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<term>Aged</term>
<term>Eye Movement Measurements</term>
<term>Female</term>
<term>Heterozygote</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Mutation</term>
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<term>Mutation</term>
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