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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
Biochem Biophys Res Commun 373(2):246252 You M et al (2015) Sirtuin 1 signaling and alcoholic fatty liver disease
P.da SilvaM
There is no single one-size-fits-all dosage for ALA, as it may be used for different purposes
