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Nature genetics, ISSN 1061-4036, 08/2019, Volume 51, Issue 8, pp. 1222 - 1232
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Tremor - pathology | Humans | Middle Aged | Fragile X Syndrome - pathology | Male | Low Density Lipoprotein Receptor-Related Protein-1 - genetics | Muscular Dystrophies - genetics | Case-Control Studies | Brain - metabolism | Adult | Female | Ataxia - genetics | High-Throughput Nucleotide Sequencing - methods | Ataxia - pathology | Fragile X Syndrome - genetics | Neuroimaging - methods | Genome-Wide Association Study | Neurodegenerative Diseases - pathology | Intranuclear Inclusion Bodies - genetics | Neurodegenerative Diseases - genetics | Genetic Markers | Muscular Dystrophies - pathology | Intranuclear Inclusion Bodies - pathology | Linkage Disequilibrium | Pedigree | Tremor - genetics | Brain - pathology | Trinucleotide Repeat Expansion - genetics | Fragile X Mental Retardation Protein - genetics | Mutation | Noncoding DNA | Neuromuscular diseases | Causes of | Nervous system | Genetic aspects | Degeneration | Nucleotide sequencing | Comparative analysis | Health aspects | DNA sequencing | Neuroimaging | Nuclear magnetic resonance--NMR | Disease | Mental disorders | Intellectual disabilities | Genomes | Leukoencephalopathy | Fragile X mental retardation protein | Neurodegeneration | Spinocerebellar ataxia | DNA methylation | Ataxia | Bioinformatics | Chromosomes | Deoxyribonucleic acid--DNA | Medical imaging | Tremor | Amyotrophic lateral sclerosis | Diseases | Neurology | Analogies | Cytomegalic inclusion disease | Insects | Fragile X syndrome | Tremors | Myopathy | Index Medicus
Journal Article
Journal of neurochemistry, ISSN 0022-3042, 04/2011, Volume 117, Issue 2, pp. 333 - 345
Journal Article