TY  - GEN
AU  - Striano,Pasquale
AU  - Iapadre,Giulia
AU  - Vari,Maria Stella
AU  - Verrotti,Alberto
TI  - Multiorgan mitochondrial dysfunction is not a main feature of MFN2 mutations (Reply to: CMT2 due to homozygous MFN2 variants is a multiorgan mitochondrial disorder)
SN  - 1532-2130
PY  - 2018///1005
KW  - Charcot-Marie-Tooth Disease
KW  - GTP Phosphohydrolases
KW  - genetics
KW  - Homozygote
KW  - Humans
KW  - Mitochondria
KW  - Mitochondrial Diseases
KW  - Mitochondrial Proteins
KW  - Mutation
N1  - Publication Type: Letter; Comment
UR  - https://doi.org/10.1016/j.ejpn.2018.04.011
ER  -