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SPTBN1 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
GEO DataSets Gene Profile neighbors Chromosome neighbors Homologene neighbors
ATP6AP2 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
WRAP73 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
TIMP3 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
PSMD13 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
KCTD12 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
MBD4 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
CDH5 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
WAPL - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
CHD7 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
SSB - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
APLP2 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
SUGP2 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
ADGRA3 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
STAG1 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
AQP1 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
NOTCH2 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
FAM98A - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
ERG - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
CLTC - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
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