Keyphrases
Mitochondrial DNA mutation
100%
Skeletal muscle
100%
Myopathy
100%
Ophthalmic Abnormalities
100%
Heteroplasmy
60%
Adult Patients
40%
Ophthalmological
40%
Ocular Motility
20%
Clinical Management
20%
Retrospective Review
20%
Clinical Presentation
20%
Molecular Diagnostics
20%
Age of Onset
20%
Mitochondrial DNA
20%
Clinical Diagnosis
20%
Nuclear Genes
20%
Mitochondrial DNA Variation
20%
Ocular Manifestations
20%
Optic Neuropathy
20%
Ophthalmology
20%
Bilateral Optic Neuropathy
20%
Gene Variants
20%
Symptom Onset
20%
Muscle Disease
20%
Pathogenic Variants
20%
Optic Nerve Disorders
20%
Muscle Tissue
20%
Mitochondrial Disease
20%
Mitochondrial DNA Maintenance
20%
Ptosis
20%
Molecular Findings
20%
Chronic Progressive External Ophthalmoplegia
20%
Genetic Clinic
20%
Optic Disc Cupping
20%
Classical Features
20%
Mitochondrial Myopathy
20%
Generalized Weakness
20%
Medicine and Dentistry
Mitochondrial DNA
100%
Myopathy
100%
Skeletal Muscle
100%
Heteroplasmy
37%
Optic Neuropathy
25%
Eye Movement
12%
Symptom
12%
Weakness
12%
Molecular Diagnosis
12%
Onset Age
12%
Disorders of Mitochondrial Functions
12%
Optic Disc
12%
Clinical Management
12%
Ophthalmology
12%
Optic Nerve
12%
Muscle Disease
12%
Ptosis
12%
Muscle Tissue
12%
Chronic Progressive External Ophthalmoplegia
12%
Mitochondrial Myopathy
12%
Biochemistry, Genetics and Molecular Biology
Mitochondrial DNA
100%
Skeletal Muscle
100%
Heteroplasmy
37%
Genetics
12%
Mitochondrial Disease
12%
Eye Movement
12%
Nuclear Gene
12%
Chronic Progressive External Ophthalmoplegia
12%
Mitochondrial Myopathy
12%