Keyphrases
CNS Effects
100%
Molecular Pathophysiology
100%
Myotonic Dystrophy
100%
Expansion mutation
75%
Molecular Mechanism
50%
RNA Gain-of-function
50%
Microsatellite Expansion
50%
Executive Function Deficits
25%
Initiation Codon
25%
Clinical Characterization
25%
Disease Mechanisms
25%
Cognitive Deficits
25%
Neuropathology
25%
Myotonic Dystrophy Type 2
25%
Clinical Consequences
25%
Clinical Phenotype
25%
Novel Protein
25%
DMPK Gene
25%
Clinically Significant
25%
Repeat-associated non-ATG Translation
25%
White Matter Integrity
25%
RNA-based
25%
MBNL2
25%
Functional Imaging
25%
Skeletal muscle
25%
CTG Expansion
25%
Genetic Characterization
25%
Postnatal Brain Development
25%
CUG Repeats
25%
Alternative Splicing
25%
DM Patients
25%
Gene Family
25%
RNA-binding Protein
25%
Biochemistry, Genetics and Molecular Biology
RNA
100%
Microsatellite
66%
Alternative Splicing
33%
Skeletal Muscle
33%
Brain Development
33%
Executive Function
33%
Intron
33%
Codon
33%
Genetics
33%
Multigene Family
33%
RNA-binding Protein
33%
Neuroscience
Myotonic Dystrophy
100%
Microsatellite
40%
Codon
20%
Intron
20%
Functional Imaging
20%
Cognitive Disorders
20%
Brain Development
20%
Skeletal Muscle
20%
Executive Function
20%
Multigene Family
20%
RNA-binding Protein
20%
Alternative Splicing
20%