Striano, Pasquale <br/><br/>
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 
<br/><br/> Publication Type: Letter; Comment 
<br/><br/><label>ISSN: </label>1532-2130 
<br/><br/><label>Standard No.: </label>10.1016/j.ejpn.2018.04.011  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Charcot-Marie-Tooth Disease<br/>GTP Phosphohydrolases--genetics<br/>Homozygote<br/>Humans<br/>Mitochondria<br/>Mitochondrial Diseases<br/>Mitochondrial Proteins--genetics<br/>Mutation