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Retrieved 15 January 2017
Glutathione synthetase deficiency is an autosomal recessive disorder that was first diagnosed in 1970 in a teenager with a slowly progressive neurologic disorder and markedly elevated excretion of 5-oxoproline in the urine, as well as a history of unexplained jaundice at birth and a history of chronic metabolic acidosis
Face: The most responsive area, with the strongest clinical evidence
Peptides Mitochondrial-derived peptide studied in metabolic, mitochondrial-function, and energy-balance research
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