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Geneva: World Health Organization
Excitation wavelength= 550 nm
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
Stimulation of bone formation and fracture healing with pulsed electromagnetic fields: Biologic responses and clinical implications
[1] Various mechanisms for the hypopigmentary effect of glutathione have been proposed, with inhibition of tyrosinase being the most important [Box 2]
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