Mitochondrial degeneration in familial ATP synthetase defect

Autor:	Vlaho, Stefan, Müller, Klaus, Selter, Mariel, Drott, Ulrich, Harter, Patrick N., Kieslich, Matthias, Mittelbronn, Michel
Jazyk:	angličtina
Rok vydání:	2012
Předmět:	ddc: 610 610 Medical sciences Medicine
Zdroj:	57th Annual Meeting of the German Society for Neuropathology and Neuroanatomy (DGNN); 20120912-20120915; Erlangen; DOC12dgnnPP1.10 /20120911/
Popis:	Mitochondrial ATP synthetase (complex V) constitutes the final pumping step for protons during ATP generation. Herein, we investigated several muscles from genetically confirmed patients with ATP synthetase defects. Lacking common alterations such as ragged-red fibers and COX-deficient fibers in histological[for full text, please go to the a.m. URL] 57th Annual Meeting of the German Society for Neuropathology and Neuroanatomy (DGNN)
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_dedup___::969a105bb0e0d69add243dcb01c9e604 http://nbn-resolving.de/urn:nbn:de:0183-12dgnn0284 Zobrazit plný text záznamu