| 000 | 01867 a2200529 4500 | ||
|---|---|---|---|
| 005 | 20250512021647.0 | ||
| 264 | 0 | _c19880113 | |
| 008 | 198801s 0 0 eng d | ||
| 022 | _a0141-8955 | ||
| 024 | 7 |
_a10.1007/BF01812849 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aScholte, H R | |
| 245 | 0 | 0 |
_aDefects in oxidative phosphorylation. Biochemical investigations in skeletal muscle and expression of the lesion in other cells. _h[electronic resource] |
| 260 |
_bJournal of inherited metabolic disease _c1987 |
||
| 300 |
_a81-97 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 | _aAdolescent |
| 650 | 0 | 4 | _aAdult |
| 650 | 0 | 4 |
_aBiotin _xmetabolism |
| 650 | 0 | 4 |
_aBrain _xenzymology |
| 650 | 0 | 4 |
_aCarnitine _xmetabolism |
| 650 | 0 | 4 | _aCells, Cultured |
| 650 | 0 | 4 | _aChild, Preschool |
| 650 | 0 | 4 |
_aCoenzyme A _xmetabolism |
| 650 | 0 | 4 | _aCytochrome-c Oxidase Deficiency |
| 650 | 0 | 4 |
_aElectron Transport Complex III _xdeficiency |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 |
_aFibroblasts _xenzymology |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aInfant |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 |
_aMetabolism, Inborn Errors _xenzymology |
| 650 | 0 | 4 |
_aMitochondria _xenzymology |
| 650 | 0 | 4 |
_aMitochondria, Liver _xenzymology |
| 650 | 0 | 4 |
_aMitochondria, Muscle _xenzymology |
| 650 | 0 | 4 |
_aMitochondrial ADP, ATP Translocases _xdeficiency |
| 650 | 0 | 4 | _aNAD(P)H Dehydrogenase (Quinone) |
| 650 | 0 | 4 | _aOxidative Phosphorylation |
| 650 | 0 | 4 |
_aQuinone Reductases _xdeficiency |
| 700 | 1 | _aBusch, H F | |
| 700 | 1 | _aLuyt-Houwen, I E | |
| 700 | 1 | _aVaandrager-Verduin, M H | |
| 700 | 1 | _aPrzyrembel, H | |
| 700 | 1 | _aArts, W F | |
| 773 | 0 |
_tJournal of inherited metabolic disease _gvol. 10 Suppl 1 _gp. 81-97 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1007/BF01812849 _zAvailable from publisher's website |
| 999 |
_c2830785 _d2830785 |
||