| 000 | 01370 a2200325 4500 | ||
|---|---|---|---|
| 005 | 20250517214532.0 | ||
| 264 | 0 | _c20181005 | |
| 008 | 201810s 0 0 eng d | ||
| 022 | _a1532-2130 | ||
| 024 | 7 |
_a10.1016/j.ejpn.2018.04.011 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aStriano, Pasquale | |
| 245 | 0 | 0 |
_aMultiorgan mitochondrial dysfunction is not a main feature of MFN2 mutations (Reply to: CMT2 due to homozygous MFN2 variants is a multiorgan mitochondrial disorder). _h[electronic resource] |
| 260 |
_bEuropean journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society _c09 2018 |
||
| 300 |
_a892-893 p. _bdigital |
||
| 500 | _aPublication Type: Letter; Comment | ||
| 650 | 0 | 4 | _aCharcot-Marie-Tooth Disease |
| 650 | 0 | 4 |
_aGTP Phosphohydrolases _xgenetics |
| 650 | 0 | 4 | _aHomozygote |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aMitochondria |
| 650 | 0 | 4 | _aMitochondrial Diseases |
| 650 | 0 | 4 |
_aMitochondrial Proteins _xgenetics |
| 650 | 0 | 4 | _aMutation |
| 700 | 1 | _aIapadre, Giulia | |
| 700 | 1 | _aVari, Maria Stella | |
| 700 | 1 | _aVerrotti, Alberto | |
| 773 | 0 |
_tEuropean journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society _gvol. 22 _gno. 5 _gp. 892-893 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1016/j.ejpn.2018.04.011 _zAvailable from publisher's website |
| 999 |
_c28378329 _d28378329 |
||