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.
ARHGEF38 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
GEO DataSets Gene Profile neighbors Chromosome neighbors Homologene neighbors
CLGN - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
ASNS - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
ATF5 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
PCK2 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
GUCA2A - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
OLFM1 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
TRIB3 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
SHMT2 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
PDE1B - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
RNF187 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
KIAA1654 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
GEO DataSets Gene Profile neighbors
SLC7A1 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
CLCN7 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
STC2 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
GDF15 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
PHGDH - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
VPS53 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
VNN2 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
RGS11 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
Filters: Manage Filters
Your browsing activity is empty.
Activity recording is turned off.
Turn recording back on