Keyphrases
Mitochondrial DNA
100%
DNA Helicase
100%
Ophthalmoplegia
100%
Familial Parkinsonism
100%
Twinkle
100%
ANT1
33%
POLG1
33%
Progressive External Ophthalmoplegia
33%
Pathogenic mutations
16%
Autosomal Dominant
16%
Proband
16%
Parkinsonism
16%
Parkinson's Disease
16%
Gene mutation
16%
Clinical Genetics
16%
Genetic Basis
16%
Exon 1
16%
Clinical Phenotype
16%
Targeted Sequencing
16%
Coding Exons
16%
Disease Phenotype
16%
Affected Family Members
16%
Neuromuscular Disease
16%
Clinical Spectrum
16%
All-affected
16%
DNA Integrity
16%
SLC25A4
16%
PEO1
16%
Medicine and Dentistry
Ophthalmoparesis
100%
Mitochondrial DNA
100%
Exon
100%
Parkinsonism
100%
Chronic Progressive External Ophthalmoplegia
100%
DNA Helicase
100%
Gene Mutation
50%
Parkinson's Disease
50%
Autosomal Dominant Inheritance
50%
Neuromuscular Disease
50%
Diseases
50%
Biochemistry, Genetics and Molecular Biology
Exon
100%
Helicase
100%
Chronic Progressive External Ophthalmoplegia
100%
Mitochondrial DNA
100%
Genetics
50%
Autosomal Dominant Inheritance
50%
Gene Mutation
50%
Proband
50%
PEO1
50%
Neuroscience
Mitochondrial DNA
100%
Ophthalmoparesis
100%
Parkinsonism
100%
DNA Helicase
100%
Exon
66%
Parkinson's Disease
33%
Gene Mutation
33%
Neuromuscular Disorder
33%