CAPN1 mutations: Expanding the CAPN1-related phenotype: From hereditary spastic paraparesis to spastic ataxia

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Publication year
2019Source
European Journal of Medical Genetics, 62, 12, (2019), article UNSP 103605ISSN
Publication type
Article / Letter to editor

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Organization
Neurology
Human Genetics
Journal title
European Journal of Medical Genetics
Volume
vol. 62
Issue
iss. 12
Subject
All institutes and research themes of the Radboud University Medical Center; Radboudumc 12: Sensory disorders DCMN: Donders Center for Medical Neuroscience; Radboudumc 3: Disorders of movement DCMN: Donders Center for Medical NeuroscienceThis item appears in the following Collection(s)
- Academic publications [227613]
- Electronic publications [107273]
- Faculty of Medical Sciences [86193]
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