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[3] In humans, defects in GSS are inherited in an autosomal recessive way and are the cause of severe metabolic acidosis, 5-oxoprolinuria, increased rate of haemolysis, and defective function of the central nervous system
Additional nanoformulations including supramolecular self-assembled structures, proteins, peptides, metal-organic frameworks, and coordination polymers will then be described
[DOI] [PubMed] [Google Scholar] 16.Bandeira L, Silva BC, Bilezikian JP
COVID-19: Can glutathione (GSH) help to reduce severe symptoms
2016;12:e1006391
