MeSH term
Frequency | Condition_Probility | English Abstract | 6 | 0.0 |
Humans | 48 | 0.0 |
Research Support, Non-U.S. Gov't | 39 | 0.0 |
Animals | 5 | 0.0 |
Charcot-Marie-Tooth Disease/diagnosis/*genetics | 2 | 16.0 |
Connexins/*genetics | 11 | 6.0 |
Female | 28 | 0.0 |
Male | 27 | 0.0 |
Myelin P0 Protein/*genetics | 18 | 62.0 |
Myelin Proteins/*genetics | 10 | 9.0 |
Pedigree | 13 | 0.0 |
Point Mutation | 3 | 0.0 |
Polymorphism, Genetic | 4 | 0.0 |
Polymorphism, Single-Stranded Conformational | 5 | 0.0 |
Adult | 17 | 0.0 |
Base Sequence | 3 | 0.0 |
Charcot-Marie-Tooth Disease/*genetics | 10 | 7.0 |
Comparative Study | 5 | 0.0 |
Connexins/genetics | 8 | 17.0 |
DNA Mutational Analysis/*methods | 3 | 2.0 |
Mutation/*genetics | 4 | 0.0 |
Myelin Proteins/genetics | 7 | 12.0 |
Research Support, U.S. Gov't, P.H.S. | 8 | 0.0 |
Sensitivity and Specificity | 2 | 0.0 |
Amino Acid Substitution | 2 | 0.0 |
DNA Primers | 2 | 0.0 |
Exons | 5 | 0.0 |
Genes, Dominant | 2 | 0.0 |
Hereditary Motor and Sensory Neuropathies/*genetics/physiopathology | 3 | 42.0 |
Chromosomes, Human, Pair 17/*genetics | 2 | 1.0 |
Cohort Studies | 3 | 0.0 |
DNA Mutational Analysis | 8 | 0.0 |
Gene Duplication | 4 | 2.0 |
Genetic Screening | 4 | 0.0 |
Genotype | 3 | 0.0 |
Hereditary Motor and Sensory Neuropathies/*genetics | 4 | 9.0 |
Italy | 2 | 0.0 |
Myelin P0 Protein/genetics | 8 | 53.0 |
Phenotype | 10 | 0.0 |
Adolescent | 4 | 0.0 |
Charcot-Marie-Tooth Disease/*genetics/pathology | 4 | 28.0 |
Child | 3 | 0.0 |
Electrophysiology | 3 | 0.0 |
*Point Mutation | 6 | 0.0 |
Amino Acid Sequence | 4 | 0.0 |
Molecular Sequence Data | 6 | 0.0 |
*Mutation | 7 | 0.0 |
Charcot-Marie-Tooth Disease/genetics/*pathology | 3 | 50.0 |
Middle Aged | 11 | 0.0 |
Myelin P0 Protein/*genetics/metabolism | 3 | 100.0 |
DNA Mutational Analysis/methods | 2 | 0.0 |
DNA-Binding Proteins/*genetics | 2 | 0.0 |
Heterozygote | 3 | 0.0 |
Homozygote | 2 | 0.0 |
Mice | 2 | 0.0 |
Chromosomes, Human, Pair 17 | 3 | 0.0 |
Myelin Sheath/*pathology | 2 | 22.0 |
Peripheral Nerves/pathology | 2 | 9.0 |
Restriction Mapping | 2 | 0.0 |
Charcot-Marie-Tooth Disease/genetics | 2 | 8.0 |
Polymerase Chain Reaction | 2 | 0.0 |
Mutation | 7 | 0.0 |
Sural Nerve/pathology | 5 | 11.0 |
Aged | 3 | 0.0 |
Biopsy | 3 | 0.0 |
Electromyography | 2 | 1.0 |
Family Health | 2 | 0.0 |
Myelin P0 Protein/chemistry/*genetics | 2 | 40.0 |
Protein Structure, Tertiary | 2 | 0.0 |
Child, Preschool | 4 | 0.0 |
Gene Deletion | 3 | 0.0 |
Age of Onset | 3 | 0.0 |
Charcot-Marie-Tooth Disease/classification/diagnosis/*genetics | 2 | 66.0 |
Multigene Family | 2 | 0.0 |
Neural Conduction | 4 | 4.0 |
X Chromosome | 2 | 0.0 |
Intestinal Absorption | 2 | 1.0 |
Charcot-Marie-Tooth Disease/*genetics/*pathology/physiopathology | 2 | 50.0 |
Axons/pathology | 2 | 6.0 |
Muscle, Skeletal/physiopathology | 2 | 10.0 |
Japan | 2 | 0.0 |