000 01228 a2200361 4500
005 20250516121645.0
264 0 _c20130314
008 201303s 0 0 eng d
022 _a1460-2075
024 7 _a10.1038/emboj.2012.300
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aKoopman, Werner J H
245 0 0 _aOXPHOS mutations and neurodegeneration.
_h[electronic resource]
260 _bThe EMBO journal
_cJan 2013
300 _a9-29 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't; Review
650 0 4 _aAnimals
650 0 4 _aCell Nucleus
_xgenetics
650 0 4 _aDNA, Mitochondrial
_xgenetics
650 0 4 _aHumans
650 0 4 _aLeigh Disease
_xgenetics
650 0 4 _aMitochondria
_xgenetics
650 0 4 _aModels, Molecular
650 0 4 _aMultienzyme Complexes
_xgenetics
650 0 4 _aMutation
_xgenetics
650 0 4 _aNeurodegenerative Diseases
_xgenetics
650 0 4 _aOxidative Phosphorylation
700 1 _aDistelmaier, Felix
700 1 _aSmeitink, Jan A M
700 1 _aWillems, Peter H G M
773 0 _tThe EMBO journal
_gvol. 32
_gno. 1
_gp. 9-29
856 4 0 _uhttps://doi.org/10.1038/emboj.2012.300
_zAvailable from publisher's website
999 _c22261550
_d22261550