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Sequence analysis of the mitochondrial genomes from Dutch pedigrees with Leber hereditary optic neuropathy
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Men with oligoasthenoteratozoospermia harbour higher numbers of multiple mitochondrial DNA deletions in their spermatozoa, but individual deletions are not indicative of overall aetiology
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Mitochondrial DNA haplogroups do not play a role in the variable phenotypic presentation of the A3243G mutation
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