MeSH term
Frequency | Condition_Probility | Amino Acid Sequence | 6 | 0.0 |
Animals | 4 | 0.0 |
Humans | 24 | 0.0 |
Mice | 3 | 0.0 |
Molecular Sequence Data | 8 | 0.0 |
Protein Structure, Tertiary | 2 | 0.0 |
Proteins/*genetics/metabolism | 2 | 0.0 |
Sequence Alignment | 4 | 0.0 |
Adolescent | 5 | 0.0 |
Adult | 13 | 0.0 |
Child | 7 | 0.0 |
Chromosomes, Human, Pair 10/genetics | 2 | 2.0 |
Epilepsy, Temporal Lobe/*genetics | 5 | 62.0 |
Female | 15 | 0.0 |
Male | 16 | 0.0 |
Middle Aged | 7 | 0.0 |
Multigene Family | 2 | 0.0 |
Research Support, Non-U.S. Gov't | 15 | 0.0 |
Sequence Homology, Amino Acid | 3 | 0.0 |
In Situ Hybridization, Fluorescence | 2 | 0.0 |
Sequence Analysis, DNA | 3 | 0.0 |
Tumor Cells, Cultured | 5 | 0.0 |
Base Sequence | 3 | 0.0 |
Chromosomes, Human, Pair 10 | 2 | 1.0 |
*Genes, Dominant | 3 | 1.0 |
Genotype | 2 | 0.0 |
*Mutation | 3 | 0.0 |
Pedigree | 11 | 0.0 |
Proteins/*genetics | 12 | 0.0 |
Research Support, U.S. Gov't, P.H.S. | 6 | 0.0 |
Reverse Transcriptase Polymerase Chain Reaction | 2 | 0.0 |
Transcription Factors/genetics | 2 | 0.0 |
Alleles | 2 | 0.0 |
DNA Mutational Analysis | 9 | 0.0 |
Epilepsy, Temporal Lobe/diagnosis/*genetics | 3 | 100.0 |
Genes, Dominant | 4 | 0.0 |
Genetic Screening | 2 | 0.0 |
Mutation/*genetics | 2 | 0.0 |
Phenotype | 4 | 0.0 |
Electroencephalography | 4 | 1.0 |
Family Health | 2 | 0.0 |
Chromosomes, Human, Pair 10/*genetics | 2 | 1.0 |
Conserved Sequence | 2 | 0.0 |
Down-Regulation | 2 | 0.0 |
*Gene Expression Regulation, Neoplastic | 2 | 0.0 |
Child, Preschool | 2 | 0.0 |
Epilepsy, Partial, Sensory/diagnosis/*genetics | 2 | 100.0 |
Family | 3 | 0.0 |
Aged | 6 | 0.0 |
*Mutation, Missense | 3 | 0.0 |
Exons/genetics | 2 | 0.0 |
Linkage (Genetics)/genetics | 2 | 0.0 |
Point Mutation/*genetics | 2 | 0.0 |
Aged, 80 and over | 2 | 0.0 |
