Keyphrases
Myoglobinuria
100%
Family Members
100%
Maternally Inherited
100%
Exercise Intolerance
100%
ND1 Gene
100%
Inherited mutation
100%
Gene mutation
100%
Homoplasmic
66%
Mitochondrial DNA
50%
Myopathy
33%
Muscle Biopsy
33%
Clinical Phenotype
16%
Rhabdomyolysis
16%
Alanine Substitution
16%
Mitochondrial Enzyme Activity
16%
PCR-sequencing
16%
Leber Hereditary Optic Neuropathy
16%
Biochemical Analysis
16%
Gene-gene
16%
Myopathic
16%
Muscle Morphology
16%
Monosymptomatic
16%
Mitochondrial Myopathy
16%
Threonine
16%
Direct Sequencing
16%
Recurrent Episodes
16%
Biochemistry, Genetics and Molecular Biology
Mitochondrial DNA
100%
Gene Mutation
100%
Mitochondrial Myopathy
33%
Alanine
33%
Electron Transport Chain
33%
Threonine
33%
Enzyme Activity
33%