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This polymorphism is in intron 13 of the MAO-B gene and is thought to disrupt monoamine metabolism, leading to increased ROS production and oxidative stress within the central nervous system (Leko et al., 2021)

Groblewska M

J Clin Endocrinol Metab (2007) 92:33303

Finally, growing evidence indicates that the role of lysosomal dysfunction in human diseases goes beyond rare inherited diseases, such as lysosomal storage disorders, to include common neurodegenerative and metabolic diseases, as well as cancer

[DOI] [PubMed] [Google Scholar] 126.Zhang X., Ren X., Zhang Q., Li Z., Ma S., Bao J., Li Z., Bai X., Zheng L., Zhang Z., et al

So, donations included the period 20122016
