Combined mineralocorticoid and glucocorticoid deficiency is caused by a novel founder nicotinamide nucleotide transhydrogenase mutation that alters mitochondrial morphology and increases oxidative stress

Ariella Weinberg-Shukron, Abdulsalam Abu-Libdeh, Fouad Zhadeh, Liran Carmel, Aviram Kogot-Levin, Lara Kamal, Moien Kanaan, Sharon Zeligson, Paul Renbaum, Ephrat Levy-Lahad, David Zangen*

*Corresponding author for this work

Research output: Contribution to journal › Article › peer-review

29 Scopus citations

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Neuroscience

Biochemistry, Genetics and Molecular Biology

Immunology and Microbiology