| 000 | 01803 a2200517 4500 | ||
|---|---|---|---|
| 005 | 20250515104946.0 | ||
| 264 | 0 | _c20080423 | |
| 008 | 200804s 0 0 eng d | ||
| 022 | _a1460-2156 | ||
| 024 | 7 |
_a10.1093/brain/awm335 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aZanna, Claudia | |
| 245 | 0 | 0 |
_aOPA1 mutations associated with dominant optic atrophy impair oxidative phosphorylation and mitochondrial fusion. _h[electronic resource] |
| 260 |
_bBrain : a journal of neurology _cFeb 2008 |
||
| 300 |
_a352-67 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 |
_aAdenosine Triphosphate _xbiosynthesis |
| 650 | 0 | 4 |
_aApoptosis _xdrug effects |
| 650 | 0 | 4 | _aCells, Cultured |
| 650 | 0 | 4 |
_aDNA Mutational Analysis _xmethods |
| 650 | 0 | 4 |
_aDNA, Mitochondrial _xanalysis |
| 650 | 0 | 4 | _aElectron Transport |
| 650 | 0 | 4 |
_aFibroblasts _xdrug effects |
| 650 | 0 | 4 |
_aGTP Phosphohydrolases _xgenetics |
| 650 | 0 | 4 | _aGene Deletion |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 |
_aMitochondria _xmetabolism |
| 650 | 0 | 4 |
_aOptic Atrophy, Autosomal Dominant _xgenetics |
| 650 | 0 | 4 |
_aOxidants _xpharmacology |
| 650 | 0 | 4 | _aOxidative Phosphorylation |
| 650 | 0 | 4 |
_aSkin _xmetabolism |
| 700 | 1 | _aGhelli, Anna | |
| 700 | 1 | _aPorcelli, Anna Maria | |
| 700 | 1 | _aKarbowski, Mariusz | |
| 700 | 1 | _aYoule, Richard J | |
| 700 | 1 | _aSchimpf, Simone | |
| 700 | 1 | _aWissinger, Bernd | |
| 700 | 1 | _aPinti, Marcello | |
| 700 | 1 | _aCossarizza, Andrea | |
| 700 | 1 | _aVidoni, Sara | |
| 700 | 1 | _aValentino, Maria Lucia | |
| 700 | 1 | _aRugolo, Michela | |
| 700 | 1 | _aCarelli, Valerio | |
| 773 | 0 |
_tBrain : a journal of neurology _gvol. 131 _gno. Pt 2 _gp. 352-67 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1093/brain/awm335 _zAvailable from publisher's website |
| 999 |
_c17730160 _d17730160 |
||