000 | 01711 a2200481 4500 | ||
---|---|---|---|
005 | 20250513075002.0 | ||
264 | 0 | _c19930916 | |
008 | 199309s 0 0 eng d | ||
022 | _a0002-9297 | ||
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aBodnar, A G | |
245 | 0 | 0 |
_aNuclear complementation restores mtDNA levels in cultured cells from a patient with mtDNA depletion. _h[electronic resource] |
260 |
_bAmerican journal of human genetics _cSep 1993 |
||
300 |
_a663-9 p. _bdigital |
||
500 | _aPublication Type: Journal Article | ||
650 | 0 | 4 | _aCell Fusion |
650 | 0 | 4 | _aCell Nucleus |
650 | 0 | 4 |
_aChromosome Aberrations _xgenetics |
650 | 0 | 4 |
_aCitrate (si)-Synthase _xdeficiency |
650 | 0 | 4 | _aCytochrome-c Oxidase Deficiency |
650 | 0 | 4 |
_aDNA, Mitochondrial _xanalysis |
650 | 0 | 4 | _aElectron Transport Complex I |
650 | 0 | 4 |
_aElectron Transport Complex IV _xgenetics |
650 | 0 | 4 |
_aFibroblasts _xenzymology |
650 | 0 | 4 | _aGene Expression Regulation, Enzymologic |
650 | 0 | 4 | _aGenetic Complementation Test |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 | _aHybrid Cells |
650 | 0 | 4 | _aInfant, Newborn |
650 | 0 | 4 |
_aMalate Dehydrogenase _xdeficiency |
650 | 0 | 4 | _aMale |
650 | 0 | 4 |
_aMitochondria _xenzymology |
650 | 0 | 4 |
_aMitochondria, Muscle _xenzymology |
650 | 0 | 4 |
_aMitochondrial Myopathies _xenzymology |
650 | 0 | 4 |
_aNADH, NADPH Oxidoreductases _xdeficiency |
650 | 0 | 4 |
_aPyruvate Dehydrogenase Complex Deficiency Disease _xgenetics |
650 | 0 | 4 |
_aSuccinate Cytochrome c Oxidoreductase _xdeficiency |
700 | 1 | _aCooper, J M | |
700 | 1 | _aHolt, I J | |
700 | 1 | _aLeonard, J V | |
700 | 1 | _aSchapira, A H | |
773 | 0 |
_tAmerican journal of human genetics _gvol. 53 _gno. 3 _gp. 663-9 |
|
999 |
_c8393919 _d8393919 |