| 000 | 01789 a2200553 4500 | ||
|---|---|---|---|
| 005 | 20250514205643.0 | ||
| 264 | 0 | _c20050110 | |
| 008 | 200501s 0 0 eng d | ||
| 022 | _a0364-5134 | ||
| 024 | 7 |
_a10.1002/ana.20278 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aLodi, Raffaele | |
| 245 | 0 | 0 |
_aDeficit of in vivo mitochondrial ATP production in OPA1-related dominant optic atrophy. _h[electronic resource] |
| 260 |
_bAnnals of neurology _cNov 2004 |
||
| 300 |
_a719-23 p. _bdigital |
||
| 500 | _aPublication Type: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 |
_aAdenosine Triphosphate _xdeficiency |
| 650 | 0 | 4 | _aAdolescent |
| 650 | 0 | 4 | _aAdult |
| 650 | 0 | 4 | _aAged |
| 650 | 0 | 4 |
_aDNA Mutational Analysis _xmethods |
| 650 | 0 | 4 |
_aExons _xgenetics |
| 650 | 0 | 4 | _aFamily Health |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 |
_aGTP Phosphohydrolases _xgenetics |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aMagnetic Resonance Spectroscopy |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aMiddle Aged |
| 650 | 0 | 4 |
_aMitochondria, Muscle _xmetabolism |
| 650 | 0 | 4 |
_aOptic Atrophy, Autosomal Dominant _xgenetics |
| 650 | 0 | 4 |
_aPhosphocreatine _xmetabolism |
| 650 | 0 | 4 | _aSequence Deletion |
| 650 | 0 | 4 | _aTime Factors |
| 700 | 1 | _aTonon, Caterina | |
| 700 | 1 | _aValentino, Maria Lucia | |
| 700 | 1 | _aIotti, Stefano | |
| 700 | 1 | _aClementi, Valeria | |
| 700 | 1 | _aMalucelli, Emil | |
| 700 | 1 | _aBarboni, Piero | |
| 700 | 1 | _aLonganesi, Lora | |
| 700 | 1 | _aSchimpf, Simone | |
| 700 | 1 | _aWissinger, Bernd | |
| 700 | 1 | _aBaruzzi, Agostino | |
| 700 | 1 | _aBarbiroli, Bruno | |
| 700 | 1 | _aCarelli, Valerio | |
| 773 | 0 |
_tAnnals of neurology _gvol. 56 _gno. 5 _gp. 719-23 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1002/ana.20278 _zAvailable from publisher's website |
| 999 |
_c15194832 _d15194832 |
||