Mutations in the gene encoding ε-sarcoglycan cause myoclonus-dystonia syndrome

Keyphrases

• Dystonia 100%
• Myoclonus 100%
• Sarcoglycan 100%
• Brain Regions 33%
• Gain-of-function mutation 33%
• DYT1 33%
• Movement Disorders 33%
• Mutated Genes 33%
• Heterogeneous Groups 33%
• Early Onset 33%
• Autosomal Dominant Disorder 33%
• Penetrance 33%
• GCH1 33%
• Writer's Cramp 33%
• Tyrosine Hydroxylase 33%
• All-affected 33%
• Alcohol 33%
• Dopa-responsive Dystonia 33%
• Arm muscles 33%
• Pedigree Analysis 33%
• Positional Cloning 33%
• GTP Cyclohydrolase I 33%
• Obsessive-compulsive Behavior 33%
• Imprinting Mechanism 33%
• Maternal Imprinting 33%
• Parent-of-origin 33%
• Torticollis 33%
• Axial muscles 33%
• Tyrosine mutant 33%
• TorsinA 33%
• DYT5 33%
• Myoclonic Jerks 33%
• DYT11 33%
• Disease Allele 33%
• Panic Attack 33%

Biochemistry, Genetics and Molecular Biology

• Sarcoglycan 100%
• SGCE 66%
• Pedigree Analysis 33%
• Torsin A 33%
• Loss of Function Mutation 33%
• Allele 33%
• Autosomal Dominant Inheritance 33%
• Mutated Genes 33%
• Penetrance 33%
• Tyrosine Hydroxylase 33%
• GTP Cyclohydrolase I 33%

Neuroscience

• Dystonia 100%
• Sarcoglycan 100%
• Myoclonus 100%
• Tyrosine Hydroxylase 14%
• Mutated Genes 14%
• Autosomal Dominant Disorder 14%
• GTP Cyclohydrolase I 14%
• Loss of Function Mutation 14%
• Compulsive Behavior 14%
• Panic Disorder 14%
• Stereotypic Movement Disorder 14%
• Brain Region 14%