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

Multiorgan mitochondrial dysfunction is not a main feature of MFN2 mutations (Reply to: CMT2 due to homozygous MFN2 variants is a multiorgan mitochondrial disorder). [electronic resource] - European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society 09 2018 - 892-893 p. digital

Publication Type: Letter; Comment

1532-2130

10.1016/j.ejpn.2018.04.011 doi


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