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

doi:10.1016/j.ejpn.2018.04.011

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

Istituto "Giannina Gaslini"

Research output: Contribution to journal › Letter › peer-review

Original language	English
Pages (from-to)	892-893
Number of pages	2
Journal	European Journal of Paediatric Neurology
Volume	22
Issue number	5
DOIs	https://doi.org/10.1016/j.ejpn.2018.04.011
Publication status	Published - Sep 1 2018

ASJC Scopus subject areas

Pediatrics, Perinatology, and Child Health
Clinical Neurology

Access to Document

10.1016/j.ejpn.2018.04.011

Cite this

Multiorgan mitochondrial dysfunction is not a main feature of MFN2 mutations (Reply to : CMT2 due to homozygous MFN2 variants is a multiorgan mitochondrial disorder). / Striano, Pasquale; Iapadre, Giulia; Vari, Maria Stella; Verrotti, Alberto.

In: European Journal of Paediatric Neurology, Vol. 22, No. 5, 01.09.2018, p. 892-893.

Research output: Contribution to journal › Letter › peer-review

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