Multiorgan mitochondrial dysfunction is not a main feature of MFN2 mutations (Reply to: CMT2 due to homozygous MFN2 variants is a multiorgan mitochondrial disorder)

Pasquale Striano, Giulia Iapadre, Maria Stella Vari, Alberto Verrotti

Research output: Contribution to journalLetterpeer-review

Original languageEnglish
Pages (from-to)892-893
Number of pages2
JournalEuropean Journal of Paediatric Neurology
Volume22
Issue number5
DOIs
Publication statusPublished - Sep 1 2018

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health
  • Clinical Neurology

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