Combined mineralocorticoid and glucocorticoid deficiency is caused by a novel founder nicotinamide nucleotide transhydrogenase mutation that alters mitochondrial morphology and increases oxidative stress (Q46715449)
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scientific article published on 12 June 2015
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Combined mineralocorticoid and glucocorticoid deficiency is caused by a novel founder nicotinamide nucleotide transhydrogenase mutation that alters mitochondrial morphology and increases oxidative stress |
scientific article published on 12 June 2015 |
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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 (English)
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Sharon Zeligson
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Ariella Weinberg-Shukron
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Abdulsalam Abu-Libdeh
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Fouad Zhadeh
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Liran Carmel
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Aviram Kogot-Levin
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Lara Kamal
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Moien Kanaan
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Paul Renbaum
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David Zangen
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12 June 2015
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52
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9
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636-641
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