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.
HMOX2 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
GEO DataSets Gene Profile neighbors Chromosome neighbors Homologene neighbors
SBF1 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
PLK3 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
PRPF40A - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
CNR1 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
KHDRBS1 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
LRRC41 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
DHX30 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
TMEM189-UBE2V1 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
GEO DataSets Gene Profile neighbors Chromosome neighbors
CTSB - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
NAGK - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
PDCD11 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
SET - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
ARHGDIA - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
GSS - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
PSMD13 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
MED12 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
EIF4G3 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
KMT2A - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
C21orf59 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
Filters: Manage Filters
Your browsing activity is empty.
Activity recording is turned off.
Turn recording back on