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- W1993347926 abstract "We report a patient who manifested a heterogeneous clinical presentation, including hypertrophic cardiomyopathy and hypothyroidism, with initially limited central nervous system involvement, and who harbored the mitochondrial (mt)DNA A3243G mutation. MtDNA analysis also revealed deleted genomes in muscle and blood. This atypical molecular combination may have influenced the clinical phenotype." @default.
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- W1993347926 date "2000-03-01" @default.
- W1993347926 modified "2023-10-13" @default.
- W1993347926 title "Combination of mtDNA mutations in a patient with a mitochondrial multisystem syndrome" @default.
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- W1993347926 doi "https://doi.org/10.1007/s100380050025" @default.
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