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Halliwell, 2006)
[21] [22] Clinical significance [edit] Patients with mutations in the GSS gene develop glutathione synthetase (GSS) deficiency, an autosomal recessive disorder
PMID: 15155329 DOI: 10.1213/01.ANE.0000113544.21754.A5 Osta WA et al (2010): Nicotinic Acetylcholine Receptor Gene Expression Is Altered in Burn Patients
