Warning: The NCBI web site requires JavaScript to function. more...
An official website of the United States government
The .gov means it's official. Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you're on a federal government site.
The site is secure. The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.
NPEPPS - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
GEO DataSets Gene Profile neighbors Chromosome neighbors Homologene neighbors
ARIH1 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
COPS5 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
RRAGA - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
NUBPL - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
CAPRIN1 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
GSTA4 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
TPRKB - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
CUL3 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
PHF10 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
KARS - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
POPDC3 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
CCNH - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
TTC1 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
ZNHIT3 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
EIF4B - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
PNPLA4 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
UBE2N - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
ST13 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
SNX1 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
Filters: Manage Filters
Your browsing activity is empty.
Activity recording is turned off.
Turn recording back on