Combined Respiratory Chain Deficiency and UQCC2 Mutations in Neonatal Encephalomyopathy: Defective Supercomplex Assembly in Complex III Deficiencies.

Autor:in

Feichtinger, René G; Brunner-Krainz, Michaela; Alhaddad, Bader; Wortmann, Saskia B; Kovacs-Nagy, Reka; Stojakovic, Tatjana; Erwa, Wolfgang; Resch, Bernhard; Windischhofer, Werner; Verheyen, Sarah; Uhrig, Sabine; Windpassinger, Christian; Locker, Felix; Makowski, Christine; Strom, Tim M; Meitinger, Thomas; Prokisch, Holger; Sperl, Wolfgang; Haack, Tobias B; Mayr, Johannes A

Schlagwörter

ATPases Associated with Diverse Cellular Activitiesgeneticsmetabolism; Blotting, Western; Carrier Proteinsgeneticsmetabolism; Electron Transport Complex IIIgeneticsmetabolism; Electrophoresis, Polyacrylamide Gel; Female; Fibroblastsmetabolism; Humans; Infant, Newborn; Membrane Proteinsgeneticsmetabolism; Mitochondrial Encephalomyopathiesgeneticsmetabolism; Mitochondrial Proteinsgeneticsmetabolism; Molecular Chaperonesgeneticsmetabolism

ISSN/eISSN

1942-0900 -

WoS ID

WOS:000406815200001