| 000 | 01745 a2200529 4500 | ||
|---|---|---|---|
| 005 | 20250514055452.0 | ||
| 264 | 0 | _c20030314 | |
| 008 | 200303s 0 0 eng d | ||
| 022 | _a0883-0738 | ||
| 024 | 7 |
_a10.1177/08830738020170101701 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aMarín-García, José | |
| 245 | 0 | 0 |
_aCardiomyopathy associated with neurologic disorders and mitochondrial phenotype. _h[electronic resource] |
| 260 |
_bJournal of child neurology _cOct 2002 |
||
| 300 |
_a759-65 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article | ||
| 650 | 0 | 4 | _aAdolescent |
| 650 | 0 | 4 |
_aCardiomyopathies _xgenetics |
| 650 | 0 | 4 | _aChild |
| 650 | 0 | 4 | _aChild, Preschool |
| 650 | 0 | 4 | _aDNA, Mitochondrial |
| 650 | 0 | 4 |
_aDystonia _xpathology |
| 650 | 0 | 4 | _aElectron Transport Complex I |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 |
_aFriedreich Ataxia _xpathology |
| 650 | 0 | 4 | _aGene Deletion |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aInfant |
| 650 | 0 | 4 | _aInfant, Newborn |
| 650 | 0 | 4 |
_aKearns-Sayre Syndrome _xpathology |
| 650 | 0 | 4 |
_aLeigh Disease _xpathology |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 |
_aMitochondria _xgenetics |
| 650 | 0 | 4 |
_aMitochondrial Myopathies _xgenetics |
| 650 | 0 | 4 |
_aMuscle, Skeletal _xpathology |
| 650 | 0 | 4 | _aMutation |
| 650 | 0 | 4 |
_aMyocardium _xpathology |
| 650 | 0 | 4 |
_aNADH, NADPH Oxidoreductases _xmetabolism |
| 650 | 0 | 4 |
_aNeuromuscular Diseases _xpathology |
| 650 | 0 | 4 |
_aOphthalmoplegia _xpathology |
| 650 | 0 | 4 | _aPhenotype |
| 650 | 0 | 4 |
_aSeizures _xpathology |
| 700 | 1 | _aGoldenthal, Michael J | |
| 700 | 1 | _aFiliano, James J | |
| 773 | 0 |
_tJournal of child neurology _gvol. 17 _gno. 10 _gp. 759-65 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1177/08830738020170101701 _zAvailable from publisher's website |
| 999 |
_c12347673 _d12347673 |
||