Combined mineralocorticoid and glucocorticoid deficiency is caused by a novel founder nicotinamide nucleotide transhydrogenase mutation that alters mitochondrial morphology and increases oxidative stress
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L. Carmel | E. Levy-Lahad | D. Zangen | M. Kanaan | Lara Kamal | P. Renbaum | S. Zeligson | Aviram Kogot-Levin | A. Weinberg-Shukron | A. Abu-Libdeh | Fouad Zhadeh