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Combined mineralocorticoid and glucocorticoid deficiency is caused by a novel founder nicotinamide nucleotide transhydrogenase mutation that alters mitochondrial morphology and increases oxidative stress
Weinberg-Shukron, A., Abu-Libdeh, A., Zhadeh, F., Carmel, L., Kogot-Levin, A., Kamal, L., Kanaan, M., Zeligson, S., Renbaum, P., Levy-Lahad, E., Zangen, D.Language:
english
Journal:
Journal of Medical Genetics
DOI:
10.1136/jmedgenet-2015-103078
Date:
June, 2015
File:
PDF, 5.15 MB
english, 2015