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UNC50 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
GEO DataSets Gene Profile neighbors Chromosome neighbors Homologene neighbors
HINT1 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
VPS26A - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
ATP6V0E1 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
FBXO28 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
TM2D3 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
SRP19 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
SUPT7L - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
ALG5 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
DST - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
PSMD6 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
RIOK3 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
BIRC2 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
HIBCH - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
NDUFB6 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
CBX1 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
EIF2B2 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
FNTA - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
SPCS2 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
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