6-OHDA	6-hydroxydopamine
acetyl-CoA	Acetyl form of coenzyme A
ADOA	Autosomal dominant optic atrophy
Cas9	CRISPR-associated protein 9
CMT2	Charcot-Marie-Tooth Type 2
CNS	Central nervous system
COA	COX assembly factor
CoQ	Coenzyme Q
COX	Cytochrome c oxidase
CRISPR	Clustered regularly interspaced short palindromic repeats
Cys	Cysteine
cyt c	cytochrome c
DNP	2-4 dinitrophenol
DOA	Dominant optic atrophy
DS	Dravet syndrome
EC	Enzyme complexes
ENU	N-ethyl-N-nitrosourea
Hcy	Homocysteine
MADD	Multiple acyl-CoA dehydrogenase deficiency
MCS	Mitochondrial carriers
MO	Morpholino oligonucleotide
MPP+	1-methyl-4-phenylpyridinium
MPTP	1-methylmethyl-4-phenylphenyl-1,2,3,6-tetrahydropyridinetetrahydropyridine
mRNA	Messenger RNA
mtDNA	Mitochondrial DNA
nDNA	Nuclear DNA
NGS	Next-generation sequencing
OxPhos	Oxidative phosphorylation
PBA	4-phenylbutyrate
PCH	Pontocerebellar hypoplasia
PD	Parkinson’s disease
PDHC	Pyruvate dehydrogenase complex
pLL	Posterior lateral line
PNS	Peripheral nervous system
ROS	Reactive oxygen species
rRNA	Ribosomal RNA
TALEN	Transcription activator-like effector
tRNA	Transfer RNA