
doi: 10.1007/bf00206061
pmid: 1757091
A good standard reference for the highly polymorphic human mitochondrial DNA (mtDNA) sequence is essential for studies of normal and disease-related nucleotide variants in the mitochondrial genome. A consensus sequence for the human mitochondrial genome has been derived from thirteen unrelated mtDNA sequences. We report 128 nucleotide variants of the human mtDNA sequence, and 62 amino acid variants of the human mitochondrial translation products, observed in the coding region of these mtDNA sequences.
Base Sequence, Databases, Factual, Gene Frequency, Consensus Sequence, Molecular Sequence Data, Mutation, Genetic Variation, Humans, Amino Acid Sequence, DNA, Mitochondrial, Mitochondria
Base Sequence, Databases, Factual, Gene Frequency, Consensus Sequence, Molecular Sequence Data, Mutation, Genetic Variation, Humans, Amino Acid Sequence, DNA, Mitochondrial, Mitochondria
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