Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations - - GEO DataSets - NCBI

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Full record GDS1065

Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations

Analysis of muscle from 12 patients with various forms of mitochondrial encephalomyopathies associated with mitochondrial DNA mutations: 8 patients with a A3243G mutation, and 4 patients with a 4977 base pair deletion. Results identify possible expression signature for mitochondrial disorders.

Organism:: Homo sapiens

Type:: Expression profiling by array, count, 3 disease state, 3 genotype/variation sets

Platform:: GPL96
Series:: GSE1462
15 Samples

Download data: CEL

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Accession:: GDS1065

ID:: 1065

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Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
Accession: GDS1065

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