aa	Amino Acid(s)
ad	Autosomal Dominant
AFP	Alpha Fetal Protein
Cas	CRISPR-associated
COS7	CV-1 Origin Sv40
CNV	Copy Number Variant
CRISPR	Clustered Regularly Interspaced Short Palindromic Repeats
CRX	Cone-Rod Homeobox
DBD	DNA Binding Domain
DSB	Double-Strand Break
EGFP	Enhanced Green Fluorescent Protein
ESCS	Enhanced S Cone Syndrome
GFAP	Glial Fibrillary Acidic Protein
gRNA	Guide RNA
HDR	Homologous-Directed Repair
HEK293	Human Embryonic Kidney
indels	Insertions/deletions
iPSC	induced Pluripotent Stem Cell
IRD	Inherited Retinal Dystrophies
KLF4	Kruppel-Like Factor
LBD	Ligand Binding Domain
LIN28A	Lin-28 Homolog A
NANOG	Nanog Homeobox
NES	Nuclear Export Signal
NHEJ	Non-Homologous End Joining
NLS	Nuclear Localization Signal
NMD	Nonsense-Mediated Decay
NR1D1	Nuclear Receptor Subfamily 1 Group D Member 1
NR2E3	Nuclear Receptor Subfamily 2 Group E Member
NRL	Neural Retina Leucine Zipper
OCT3/4	Octamer Binding Transcription Factor
OTX2	Orthodenticle Homeobox 2
PAM	Protospacer Adjacent Motif
PTC	Premature Termination Codon
RP	Retinitis Pigmentosa
SeV	Sendai Virus
SMA	Smooth Muscle Actin
SOX2	SRY-Box Transcription Factor 2
Sp	Streptococcus Pyogenes
T7E1	T7 Endonuclease 1
WT	Wild type