| Phylogenetic analysis of mitochondrial DNA: Detection of mutations in patients with occipital stroke | ||
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adenosine diphosphate
adenine nucleotide translocator
adenosine triphosphate
base pair
coenzyme Q10
cytochrome c oxidase
(chronic) progressive external ophthalmoplegia
conformation sensitive gel electrophoresis
cytochrome c
displacement loop
deoxyribonucleic acid
electron transfer chain
hereditary spastic paraplegia
hypervariable segment
Leber’s hereditary optic neuropathy
mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes
myoclonus epilepsy with ragged-red fibers
maternally inherited Leigh syndrome
messenger RNA
mitochondrial DNA
transcription termination factor
reduced nicotinamide adenine dinucleotide
neurogenic weakness, ataxia and retinitis pigmentosa
nucleotide
origin of replication of the heavy strand of mtDNA
origin of replication of the light strand of mtDNA
oxidative phosphorylation
polymerase chain reaction
mtDNA transcription initiation site in the heavy strand
inorganic phosphate
mtDNA transcription initiation site in the light strand
restriction fragment length polymorphism
ribonucleic acid
ragged-red fiber
ribosomal ribonucleic acid
succinate dehydrogenase
tricarboxylic acid
transfer ribonucleic acid
years before present