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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

USA 93 , 79237926 (1996)

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doi: 10.1016/j.ecoenv.2021.112947 150 YuanATStillmanMJ