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Niacin-responsive genetic disorders Congenital NAD deficiency-related disorders can result from mutations in genes involved in the uptake and transport of the various dietary NAD + precursors or in the distinct metabolic pathways leading to NAD + production (see Metabolism)
Pomatto, L
Gurung et al., 2020)
The Pickart & Margolina 2018 review documented its extensive gene-modulating effects, and the AHK-Cu 2007 study tested a related variant on hair follicles in the lab
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