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A homozygous glutathione peroxidase 1 mutation, p. Arg130-Leu133del, in a patient with familial glucocorticoid deficiency
A homozygous glutathione peroxidase 1 mutation, p. Arg130-Leu133del, in a patient with familial glucocorticoid deficiency
2012
Julia Kowalczyk
Eirini Meimaridou
Leonardo Guasti
Peter Nürnberg
Philippe Touraine
Peter King
Lou Metherell
Keywords:
GPX1
Familial Glucocorticoid Deficiency
Endocrinology
Mutation
Medicine
Internal medicine
Correction
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