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Familial Glucocorticoid Deficiency: New Genes and Mechanisms
(Queen Mary University of London, 08/04/2014)
Mutations in the melanocortin 2 receptor (MC2R) and its accessory protein (MRAP), in the ACTH signalling pathway, and the antioxidant genes nicotinamide nucleotide transhydrogenase (NNT) and thioredoxin reductase 2 (TXNRD2) ...