KIF1A variants are a frequent cause of autosomal dominant hereditary spastic paraplegia
SourceEuropean Journal of Human Genetics, 28, 1, (2020), pp. 40-49
Article / Letter to editor
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European Journal of Human Genetics
SubjectAll 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 Neuroscience; Radboudumc 7: Neurodevelopmental disorders DCMN: Donders Center for Medical Neuroscience; Radboudumc 9: Rare cancers RIHS: Radboud Institute for Health Sciences
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