Eye movement disorders in ATP13A2 mutation carriers (PARK9)

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Published in	Movement disorders Vol. 25; no. 15; pp. 2687 - 2689
Main Authors	Machner, Björn, Sprenger, Andreas, Behrens, Maria Isabel, Ramirez, Alfredo, Brüggemann, Norbert, Klein, Christine, Helmchen, Christoph
Format	Journal Article
Language	English
Published	Hoboken Wiley Subscription Services, Inc., A Wiley Company 15.11.2010 Wiley Wiley Subscription Services, Inc
Subjects	Adult Aged Biological and medical sciences Chile Diseases of striated muscles. Neuromuscular diseases Eye Movement Measurements Eye Movements - genetics Female Heterozygote Humans Male Medical sciences Middle Aged Mutation Neurology Ocular Motility Disorders - genetics Proton-Translocating ATPases - genetics Chile Nervous system diseases Mutation Carrier Eye movement
Online Access	Get full text
ISSN	0885-3185 1531-8257 1531-8257
DOI	10.1002/mds.23352

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Author	Ramirez, Alfredo Brüggemann, Norbert Klein, Christine Machner, Björn Sprenger, Andreas Helmchen, Christoph Behrens, Maria Isabel
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References	e_1_2_1_3_1_6_2 e_1_2_1_3_1_7_2 e_1_2_1_3_1_8_2 e_1_2_1_3_1_2_2 Behrens MI (e_1_2_1_3_1_4_2) e_1_2_1_3_1_3_2 Brüggemann N (e_1_2_1_3_1_5_2)
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SubjectTerms	Adult Aged Biological and medical sciences Chile Diseases of striated muscles. Neuromuscular diseases Eye Movement Measurements Eye Movements - genetics Female Heterozygote Humans Male Medical sciences Middle Aged Mutation Neurology Ocular Motility Disorders - genetics Proton-Translocating ATPases - genetics
Title	Eye movement disorders in ATP13A2 mutation carriers (PARK9)
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