000 01115 a2200313 4500
005 20250515155746.0
264 0 _c20090421
008 200904s 0 0 eng d
022 _a1365-2796
024 7 _a10.1111/j.1365-2796.2008.02059.x
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aSpinazzola, A
245 0 0 _aDisorders from perturbations of nuclear-mitochondrial intergenomic cross-talk.
_h[electronic resource]
260 _bJournal of internal medicine
_cFeb 2009
300 _a174-92 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAnimals
650 0 4 _aDNA, Mitochondrial
_xgenetics
650 0 4 _aDisease Models, Animal
650 0 4 _aGene Deletion
650 0 4 _aHumans
650 0 4 _aMice
650 0 4 _aMitochondrial Diseases
_xclassification
650 0 4 _aMutation
_xgenetics
650 0 4 _aOxidative Phosphorylation
700 1 _aZeviani, M
773 0 _tJournal of internal medicine
_gvol. 265
_gno. 2
_gp. 174-92
856 4 0 _uhttps://doi.org/10.1111/j.1365-2796.2008.02059.x
_zAvailable from publisher's website
999 _c18636869
_d18636869