MeSH term
Frequency | Condition_Probility | Humans | 16 | 0.0 |
Cells, Cultured | 2 | 0.0 |
*Mutation | 4 | 0.0 |
Research Support, Non-U.S. Gov't | 12 | 0.0 |
Research Support, U.S. Gov't, P.H.S. | 11 | 0.0 |
DNA, Mitochondrial/*genetics | 5 | 4.0 |
Adult | 3 | 0.0 |
Exons | 2 | 0.0 |
Female | 4 | 0.0 |
Genes, Recessive | 4 | 0.0 |
Introns | 2 | 0.0 |
Male | 6 | 0.0 |
Middle Aged | 3 | 0.0 |
Mitochondrial Encephalomyopathies/*genetics | 4 | 100.0 |
Point Mutation | 3 | 0.0 |
Sequence Deletion | 3 | 0.0 |
Syndrome | 2 | 0.0 |
Thymidine Phosphorylase/*genetics | 4 | 80.0 |
Amino Acid Sequence | 2 | 0.0 |
Mitochondrial Encephalomyopathies/enzymology/*genetics | 2 | 100.0 |
Molecular Sequence Data | 3 | 0.0 |
Thymidine/metabolism | 3 | 0.0 |
Blotting, Southern | 4 | 0.0 |
*Gene Deletion | 2 | 0.0 |
Polymerase Chain Reaction | 3 | 0.0 |
Adolescent | 3 | 0.0 |
Chromatography, High Pressure Liquid | 2 | 0.0 |
Mutation | 2 | 0.0 |
Thymidine Phosphorylase/*deficiency/*genetics | 2 | 100.0 |
Deoxyuridine/metabolism | 2 | 25.0 |
Models, Genetic | 2 | 0.0 |
Sequence Analysis, DNA | 2 | 0.0 |
Gastrointestinal Diseases/genetics | 2 | 66.0 |
