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Description
[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

Riber, L

Clearance of autophagy-associated dying retinal pigment epithelial cellsa possible source for inflammation in age-related macular degeneration
[DOI] [PubMed] [Google Scholar] 136.Dimitriadis F., Borgmann H., Struck J.P., Salem J., Kuru T.H
