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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

Authors

  1. Correspondence to Professor David Zangen, Division of Pediatric Endocrinology, Hadassah Hebrew University Medical Center, Jerusalem 91240, Israel; zangend{at}hadassah.org.il
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Citation

Weinberg-Shukron A, Abu-Libdeh A, Zhadeh F, et al
Combined mineralocorticoid and glucocorticoid deficiency is caused by a novel founder nicotinamide nucleotide transhydrogenase mutation that alters mitochondrial morphology and increases oxidative stress

Publication history

  • Received February 19, 2015
  • Revised May 17, 2015
  • Accepted May 24, 2015
  • First published June 12, 2015.
Online issue publication 
August 21, 2015

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