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Mitochondrial DNA mutations in patients with myelodysplastic syndromes

2 Apr 2003

Abstract excerpt

We undertook to systematically analyze the entire mitochondrial genome by gene amplification and direct sequencing in 10 patients with myelodysplasia; results were compared with concomitantly studied 8 healthy volunteers as well as mtDNA sequences in a standard database. Nucleotide changes that were present in our healthy controls as well as those in published databases were counted as polymorphisms. Overall,...

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Identifiers

PMID: 12446454
DOI: 10.1182/blood-2002-06-1825

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