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008 231108 ||| eng
100 1 |a Winter, Monika 
245 0 0 |a Aetiology and molecular genetic basis of OXPHOS deficiencies  |h Elektronische Ressource  |c Monika Winter 
246 3 1 |a Etiology and molecular genetic basis of OXPHOS deficiencies 
260 |a London  |b Henry Stewart Talks  |c 2023, 2023 
300 |a 1 streaming video file (34 min.)  |b color, sound 
505 0 |a Contents: Cellular metabolism -- Mitochondrial metabolism -- OXPHOS system -- Mito-nuclear cross-talk -- The complexity of complex I assembly -- Structural organization of OXPHOS complexes -- Mitochondrial disease genes -- Mitochondrial disease -- Functional investigation of NDUFC2 variants 
653 |a Mitochondrial Diseases / pathology 
653 |a NDUFC2 protein, human 
653 |a Mitochondrial pathology 
653 |a Metabolism / Disorders 
653 |a Mitochondria 
653 |a Energy Metabolism 
653 |a Phosphorylation 
653 |a Oxidative Phosphorylation 
653 |a Oxidation, Physiological 
653 |a Genes, Mitochondrial 
653 |a Mitochondria / metabolism 
653 |a Electron Transport Complex I. 
653 |a Mitochondrial Diseases / genetics 
041 0 7 |a eng  |2 ISO 639-2 
989 |b HST  |a Henry Stewart Talks 
490 0 |a Mitochondria in health and disease 
500 |a Animated audio-visual presentation with synchronized narration. - Title from title frames. - Mode of access: World Wide Web 
856 4 2 |u https://hstalks.com/bs/p/1034  |3 Series 
856 4 0 |u https://hstalks.com/bs/5434  |x Verlag  |z Streaming video file 
082 0 |a 570