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.
HMGB3P1 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
GEO DataSets Gene Profile neighbors Chromosome neighbors
NDC80 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
GEO DataSets Gene Profile neighbors Chromosome neighbors Homologene neighbors
PDE9A - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
PLD2 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
VIPR2 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
CALML4 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
NR2F2 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
FBXO11 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
NACAP1 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
UROD - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
PPIL2 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
RBPMS - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
IGLC1 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
SNX29 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
N4BP2L2 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
GGCX - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
DCN - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
HIF1A - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
HADHA - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
CTBP2 - Mitochondrial encephalomyopathies associated with mitochondrial DNA mutations
Filters: Manage Filters
Your browsing activity is empty.
Activity recording is turned off.
Turn recording back on