Niemann-Pick type C (NPC)1 disease is a rare genetic condition in which the function of the lysosomal cholesterol transporter NPC1 protein is impaired. Consequently. sphingolipids and cholesterol accumulate in lysosomes of all tissues. triggering a cascade of pathological events that culminate in severe systemic and neurological symptoms. https://parisnaturalfoodes.shop/product-category/living-mustard/
Dietary plant stanol ester supplementation reduces peripheral symptoms in a mouse model of Niemann-Pick type C1 disease[S]
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