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

Eur J Paediatr Neurol. 2018 Sep;22(5):892-893. doi: 10.1016/j.ejpn.2018.04.011. Epub 2018 Apr 30.

Authors

Pasquale Striano¹, Giulia Iapadre², Maria Stella Vari¹, Alberto Verrotti³

Affiliations

¹ Pediatric Neurology and Muscular Diseases Unit, Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, "G. Gaslini" Institute, Genova, Italy.
² Department of Pediatrics, University of L'Aquila, L'Aquila, Italy.
³ Department of Pediatrics, University of L'Aquila, L'Aquila, Italy. Electronic address: [email protected].

PMID: 29748043
DOI: 10.1016/j.ejpn.2018.04.011

No abstract available

Publication types

Letter
Comment

MeSH terms

Charcot-Marie-Tooth Disease*
GTP Phosphohydrolases / genetics
Homozygote*
Humans
Mitochondria
Mitochondrial Diseases
Mitochondrial Proteins / genetics
Mutation

Substances

Mitochondrial Proteins
GTP Phosphohydrolases
MFN2 protein, human