Movement Disorders (revue)

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Eye movement disorders in ATP13A2 mutation carriers (PARK9)

Identifieur interne : 001C93 ( Main/Exploration ); précédent : 001C92; suivant : 001C94

Eye 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 :

RBID : ISTEX:01069E3312E004211146729FB28B2423B3886932

Descripteurs français

English descriptors


Url:
DOI: 10.1002/mds.23352


Affiliations:


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<term>Eye Movement Measurements</term>
<term>Eye Movements (genetics)</term>
<term>Eye movement</term>
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<term>Heterozygote</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
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<term>Nervous system diseases</term>
<term>Ocular Motility Disorders (genetics)</term>
<term>Proton-Translocating ATPases (genetics)</term>
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