List of bibliographic references
Number of relevant bibliographic references: 6.
List of associated KwdEn.i
Nombre de
documents | Descripteur |
|---|
| 6 | Humans |
| 4 | Adolescent |
| 4 | Female |
| 4 | Male |
| 3 | Adult |
| 3 | Aged |
| 3 | Middle Aged |
| 3 | Nervous system diseases |
| 3 | Young Adult |
| 2 | Child |
| 2 | DNA Mutational Analysis |
| 2 | Essential Tremor (genetics) |
| 2 | Family Health |
| 2 | Genetic Linkage |
| 2 | Genotype |
| 2 | Human |
| 2 | Lod Score |
| 2 | Mutation |
| 2 | Paraplegia (genetics) |
| 2 | Pedigree |
| 2 | Tremor |
| 1 | 14q22–q24 |
| 1 | Age of Onset |
| 1 | Aged, 80 and over |
| 1 | Anticipation, Genetic |
| 1 | Atrophy (complications) |
| 1 | Chi-Square Distribution |
| 1 | Child, Preschool |
| 1 | Chromosome Aberrations |
| 1 | Chromosome Mapping |
| 1 | Chromosomes, Human, Pair 14 (genetics) |
| 1 | Chromosomes, Human, Pair 15 (genetics) |
| 1 | Chromosomes, Human, Pair 16 |
| 1 | Chromosomes, Human, Pair 3 (genetics) |
| 1 | Chromosomes, Human, Y (genetics) |
| 1 | Corpus Callosum (pathology) |
| 1 | Corpus callosum |
| 1 | Essential |
| 1 | Essential Tremor (epidemiology) |
| 1 | Europe |
| 1 | Europe (epidemiology) |
| 1 | European Continental Ancestry Group (genetics) |
| 1 | European samples |
| 1 | Exons (genetics) |
| 1 | Family study |
| 1 | Gene |
| 1 | Gene Frequency |
| 1 | Genes, Dominant |
| 1 | Genetic Association Studies (methods) |
| 1 | Genetic Markers |
| 1 | Genetic Predisposition to Disease |
| 1 | Genetic Predisposition to Disease (genetics) |
| 1 | Genetic determinism |
| 1 | Genetic linkage |
| 1 | Genetics, Population |
| 1 | Genome-Wide Association Study (methods) |
| 1 | Guanine Nucleotide Exchange Factors (genetics) |
| 1 | Haplotypes |
| 1 | Hereditary spastic paraplegia |
| 1 | Heterogeneity |
| 1 | Kjellin's syndrome |
| 1 | LINGO1 |
| 1 | Linkage |
| 1 | Locus |
| 1 | Magnetic Resonance Imaging |
| 1 | Membrane Proteins (genetics) |
| 1 | Molecular biology |
| 1 | Mutation (genetics) |
| 1 | Nerve Tissue Proteins (genetics) |
| 1 | Neurodegenerative Diseases (genetics) |
| 1 | Pantothenate kinase |
| 1 | Paraplegia (complications) |
| 1 | Paraplegia (physiopathology) |
| 1 | Phenotype |
| 1 | Phosphotransferases (Alcohol Group Acceptor) (genetics) |
| 1 | Point Mutation (genetics) |
| 1 | Polymorphism |
| 1 | Polymorphism, Single Nucleotide (genetics) |
| 1 | Proteins (genetics) |
| 1 | SPG15 |
| 1 | Severity of Illness Index |
| 1 | Spectrin (genetics) |
| 1 | Spinocerebellar Ataxias (diagnosis) |
| 1 | Spinocerebellar Ataxias (genetics) |
| 1 | Tajikistan |
| 1 | Tunisia (epidemiology) |
| 1 | association study |
| 1 | essential tremor |
| 1 | hereditary spastic paraplegia |
| 1 | linkage |
| 1 | movement disorder |
| 1 | thin corpus callosum |
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