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Title:

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

Document type:
Journal Article; Article
Author(s):
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
Abstract:
Vertebrate respiratory chain complex III consists of eleven subunits. Mutations in five subunits either mitochondrial (MT-CYB) or nuclear (CYC1, UQCRC2, UQCRB, and UQCRQ) encoded have been reported. Defects in five further factors for assembly (TTC19, UQCC2, and UQCC3) or iron-sulphur cluster loading (BCS1L and LYRM7) cause complex III deficiency. Here, we report a second patient with UQCC2 deficiency. This girl was born prematurely; pregnancy was complicated by intrauterine growth retardation...     »
Journal title abbreviation:
Oxid Med Cell Longev
Year:
2017
Journal volume:
2017
Pages contribution:
7202589
Language:
eng
Fulltext / DOI:
doi:10.1155/2017/7202589
Pubmed ID:
http://view.ncbi.nlm.nih.gov/pubmed/28804536
Print-ISSN:
1942-0900
TUM Institution:
Institut für Humangenetik; Klinik und Poliklinik für Kinderheilkunde und Jugendmedizin
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