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Homozygous Expression of Mutant ELOVL4 Leads to Seizures and Death in a Novel Animal Model of Very Long-Chain Fatty Acid Deficiency.
The Elovl4 Spinocerebellar Ataxia-34 Mutation 736T>G (p.W246G) Impairs Retinal Function in the Absence of Photoreceptor Degeneration.
Vesicle-associated membrane protein isoforms in the tiger salamander retina.
CNGA3 deficiency affects cone synaptic terminal structure and function and leads to secondary rod dysfunction and degeneration.
Differential distribution of synaptotagmin immunoreactivity among synapses in the goldfish, salamander, and mouse retina.
Differential distribution of vesicle associated membrane protein isoforms in the mouse retina.
SV2B regulates synaptotagmin 1 by direct interaction.
Very long chain polyunsaturated fatty acids and rod cell structure and function.
Synaptic protein expression by regenerating adult photoreceptors.
W246G Mutant ELOVL4 Impairs Synaptic Plasticity in Parallel and Climbing Fibers and Causes Motor Defects in a Rat Model of SCA34.