Alexander disease causing hereditary late-onset ataxia with only minimal white matter changes: A report of two sibs.

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Publication year
2008Source
Movement Disorders, 23, 11, (2008), pp. 1613-5ISSN
Publication type
Article / Letter to editor

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Organization
Neurology
Journal title
Movement Disorders
Volume
vol. 23
Issue
iss. 11
Page start
p. 1613
Page end
p. 5
Subject
DCN 2: Functional Neurogenomics; UMCN 3.2: Cognitive neurosciencesThis item appears in the following Collection(s)
- Academic publications [229134]
- Electronic publications [111496]
- Faculty of Medical Sciences [87758]
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