Ataxia oculomotor apraxia type 2: course over 27 years and a novel stop mutation in the senataxin gene

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Published in:Journal of neurology 2009-09, Vol.256 (9), p.1555-1557
Main Authors: Haack, Tobias, Friday, Douglas, Bender, Andreas, Rolfs, Arndt, Klopstock, Thomas
Format: Article
Language:English
Subjects:
Apraxias - diagnosis
Apraxias - genetics
Apraxias - pathology
Ataxia - diagnosis
Ataxia - genetics
Ataxia - pathology
Brain - pathology
Diagnosis, Differential
Disease Progression
Female
Humans
Letter to the Editors
Magnetic Resonance Imaging
Medicine
Medicine & Public Health
Middle Aged
Mutation
Neurology
Neuroradiology
Neurosciences
Ocular Motility Disorders - diagnosis
Ocular Motility Disorders - genetics
Ocular Motility Disorders - pathology
RNA Helicases - genetics
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cites cdi_FETCH-LOGICAL-c338t-9bbcbfc0c8e7ce0060e6e84f71ac0b081a648ae6fa6f94fc2aff618e8cbbf8773
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container_issue 9
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container_title Journal of neurology
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creator Haack, Tobias
Friday, Douglas
Bender, Andreas
Rolfs, Arndt
Klopstock, Thomas
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doi_str_mv 10.1007/s00415-009-5133-3
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identifier ISSN: 0340-5354
ispartof Journal of neurology, 2009-09, Vol.256 (9), p.1555-1557
issn 0340-5354
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source Springer Nature
subjects Apraxias - diagnosis
Apraxias - genetics
Apraxias - pathology
Ataxia - diagnosis
Ataxia - genetics
Ataxia - pathology
Brain - pathology
Diagnosis, Differential
Disease Progression
Female
Humans
Letter to the Editors
Magnetic Resonance Imaging
Medicine
Medicine & Public Health
Middle Aged
Mutation
Neurology
Neuroradiology
Neurosciences
Ocular Motility Disorders - diagnosis
Ocular Motility Disorders - genetics
Ocular Motility Disorders - pathology
RNA Helicases - genetics
title Ataxia oculomotor apraxia type 2: course over 27 years and a novel stop mutation in the senataxin gene
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