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Original research
Mutation in the MICOS subunit gene APOO (MIC26) associated with an X-linked recessive mitochondrial myopathy, lactic acidosis, cognitive impairment and autistic features

Authors

  1. Correspondence to Professor Massimo Zeviani, Mitochondrial Biology Unit, Medical Research Council, Cambridge, CB2 0XY, UK; massimo.zeviani{at}unipd.it
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Citation

Benincá C, Zanette V, Brischigliaro M, et al
Mutation in the MICOS subunit gene APOO (MIC26) associated with an X-linked recessive mitochondrial myopathy, lactic acidosis, cognitive impairment and autistic features

Publication history

  • Received January 14, 2020
  • Revised March 13, 2020
  • Accepted April 12, 2020
  • First published May 21, 2020.
Online issue publication 
February 18, 2021

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