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The International journal of developmental biology, ISSN 0214-6282, 01/2020, Volume 64, Issue 7-9, pp. 445 - 452
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Journal of the neurological sciences, ISSN 0022-510X, 1996, Volume 142, Issue 1-2, pp. 140 - 147
MRI | anticipation | SCA1 | SCA2 | autosomal dominant cerebellar ataxia | Neurosciences | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Neurology | Biological and medical sciences | Medical sciences | Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases | Humans | Middle Aged | Child, Preschool | Electrophysiology | Genotype | Male | Chromosome Disorders | Mutation - genetics | Disease Progression | Cerebellar Ataxia - physiopathology | Phenotype | Cerebellar Ataxia - genetics | Adolescent | Age of Onset | Chromosome Aberrations | Adult | Female | Italy | Cerebellar Ataxia - diagnosis | Child | Genetic Linkage | Medicine, Experimental | Brain | Medical research | Genetic aspects | Cerebellar ataxia | Neurophysiology | Index Medicus
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