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Ferrante RJ, Klein AM, et al
[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
Comparative investigation of differential mood responses among elite, non-elite, and non-athletes in total lockdown
10.1038/s41419-017-0033-4 383 YoshinoJ.BaurJ
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