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Description
Additionally, TMAO has been connected to a higher prevalence of metabolic syndrome and T2D
Neuronal ceroid lipofuscinoses (NCLs) are a group of autosomal-recessive hereditary lysosomal storage diseases caused by mutations in at least 8 genes (CLN1-CLN8) [115]
Clinically, personalized treatment strategies could be developed by integrating modern medicine with TCM or combining herbal and synthetic drugs to enhance therapeutic efficacy and improve patient outcomes
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Skadniki: fumaran L-karnityny, acetyl-L-karnityna
