Title : SARM1 depletion rescues NMNAT1-dependent photoreceptor cell death and retinal degeneration.

Pub. Date : 2020 Oct 27

PMID : 33107823






1 Functional Relationships(s)
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1 Leber congenital amaurosis type nine is an autosomal recessive retinopathy caused by mutations of the NAD+ synthesis enzyme NMNAT1. NAD nicotinamide nucleotide adenylyltransferase 1 Homo sapiens