APA

Striano P., Iapadre G., Vari M. S. & Verrotti A. (20181005). Multiorgan mitochondrial dysfunction is not a main feature of MFN2 mutations (Reply to: CMT2 due to homozygous MFN2 variants is a multiorgan mitochondrial disorder). : European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Chicago

Striano Pasquale, Iapadre Giulia, Vari Maria Stella and Verrotti Alberto. 20181005. Multiorgan mitochondrial dysfunction is not a main feature of MFN2 mutations (Reply to: CMT2 due to homozygous MFN2 variants is a multiorgan mitochondrial disorder). : European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Harvard

Striano P., Iapadre G., Vari M. S. and Verrotti A. (20181005). Multiorgan mitochondrial dysfunction is not a main feature of MFN2 mutations (Reply to: CMT2 due to homozygous MFN2 variants is a multiorgan mitochondrial disorder). : European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

MLA

Striano Pasquale, Iapadre Giulia, Vari Maria Stella and Verrotti Alberto. Multiorgan mitochondrial dysfunction is not a main feature of MFN2 mutations (Reply to: CMT2 due to homozygous MFN2 variants is a multiorgan mitochondrial disorder). : European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society. 20181005.