MeSH term
Frequency | Condition_Probility | Female | 26 | 0.0 |
Humans | 41 | 0.0 |
Middle Aged | 20 | 0.0 |
Adenosinetriphosphatase/*genetics | 12 | 12.0 |
DNA Mutational Analysis | 7 | 0.0 |
Male | 25 | 0.0 |
Pedigree | 19 | 0.0 |
Polymerase Chain Reaction | 5 | 0.0 |
Polymorphism, Genetic | 2 | 0.0 |
Polymorphism, Single-Stranded Conformational | 2 | 0.0 |
Research Support, Non-U.S. Gov't | 31 | 0.0 |
Spastic Paraplegia, Hereditary/*genetics | 14 | 46.0 |
English Abstract | 2 | 0.0 |
Genotype | 3 | 0.0 |
Phenotype | 8 | 0.0 |
Adult | 22 | 0.0 |
Chromosome Mapping | 5 | 0.0 |
Genes, Dominant/genetics | 2 | 1.0 |
Genetic Heterogeneity | 3 | 1.0 |
Magnetic Resonance Imaging | 2 | 0.0 |
Amino Acid Sequence | 2 | 0.0 |
Base Sequence | 4 | 0.0 |
Chromosomes, Human, Pair 2/genetics | 2 | 1.0 |
Cloning, Molecular | 3 | 0.0 |
Contig Mapping | 4 | 2.0 |
GTP Phosphohydrolases/*genetics | 2 | 5.0 |
Lod Score | 7 | 0.0 |
Molecular Sequence Data | 4 | 0.0 |
Mutation/*genetics | 6 | 0.0 |
RNA, Messenger/genetics/metabolism | 2 | 0.0 |
Research Support, U.S. Gov't, Non-P.H.S. | 3 | 0.0 |
Research Support, U.S. Gov't, P.H.S. | 8 | 0.0 |
Reverse Transcriptase Polymerase Chain Reaction | 4 | 0.0 |
Sequence Alignment | 2 | 0.0 |
Sequence Homology, Amino Acid | 2 | 0.0 |
*Chromosomes, Human, Pair 2 | 2 | 0.0 |
Adolescent | 9 | 0.0 |
Age of Onset | 8 | 0.0 |
Aged | 10 | 0.0 |
Animals | 3 | 0.0 |
Child | 8 | 0.0 |
Child, Preschool | 6 | 0.0 |
Exons/genetics | 6 | 0.0 |
Infant | 2 | 0.0 |
Introns/genetics | 3 | 0.0 |
Linkage (Genetics)/genetics | 4 | 1.0 |
Paraparesis, Spastic/*genetics | 2 | 100.0 |
Chromosomes, Human, Pair 2/*genetics | 6 | 3.0 |
Family Health | 4 | 0.0 |
Sequence Analysis, DNA | 3 | 0.0 |
Trinucleotide Repeats/*genetics | 3 | 3.0 |
Italy | 2 | 0.0 |
Polymorphism, Restriction Fragment Length | 2 | 0.0 |
Mutation/genetics | 2 | 0.0 |
DNA/genetics | 3 | 0.0 |
Fluorescent Antibody Technique | 2 | 0.0 |
*Genes, Dominant | 4 | 1.0 |
Microsatellite Repeats | 4 | 0.0 |
DNA Primers | 2 | 0.0 |
Microtubules/*metabolism | 2 | 2.0 |
*Chromosome Mapping | 3 | 0.0 |
Genes, Dominant/*genetics | 3 | 3.0 |
Haplotypes/genetics | 3 | 0.0 |
Adenosinetriphosphatase/*genetics/physiology | 2 | 66.0 |
*Mutation | 3 | 0.0 |
Paraplegia/*genetics | 5 | 45.0 |
Aged, 80 and over | 4 | 0.0 |
Amino Acid Motifs | 2 | 0.0 |
Expressed Sequence Tags | 4 | 0.0 |
Calcium-Binding Proteins/*genetics | 3 | 3.0 |
Chromosomes, Artificial, Yeast | 2 | 0.0 |
Genes, Dominant | 4 | 0.0 |
*Mutation, Missense | 2 | 0.0 |
Linkage (Genetics) | 5 | 0.0 |
Haplotypes | 2 | 0.0 |
Chromosomes, Human, Pair 14 | 2 | 1.0 |
Chromosomes, Human, Pair 2 | 2 | 1.0 |
Genetic Markers/genetics | 2 | 0.0 |
Comparative Study | 4 | 0.0 |
Mutation | 2 | 0.0 |
Germany | 2 | 0.0 |
DNA Mutational Analysis/*methods | 2 | 1.0 |
RNA, Messenger/biosynthesis | 2 | 0.0 |