Article info

Download PDFPDF

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
View Full Text

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.

Request permissions

If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.