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[21] [22] Clinical significance [edit] Patients with mutations in the GSS gene develop glutathione synthetase (GSS) deficiency, an autosomal recessive disorder

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Tanphaichitr VS, Pung-amrit P, Yodthong S, Soongswang J, Mahasandana C, Suvatte V: Glucose-6-phosphate dehydrogenase deficiency in the newborn: its prevalence and relation to neonatal jaundice

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What made his discovery remarkable was the observation that this small molecule caused old liver tissue to synthesize proteins like younger tissue

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