Zellweger Syndrome coupled to secondary mitochondrial cytopathy in skeletal muscle cells in an infant: a pattern of biochemical overlapping in metabolic myopathies

Autor:	Salpietro, V, Phadke, R, Saggar, A, Yates, R, Fokoloros, C, Mankad, K, Hertecant, J, Ruggieri, M, Mccormick, D, Kinali, M.
Jazyk:	angličtina
Rok vydání:	2015
Předmět:	Zellweger syndrome . Metabolic myopathy . Peroxisomal biogenesis . Disorders . Mitochondrial dysfunction . PEX16 . PEX 12
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=od______4731::c09acf6e872f0dee8258e100b17653bd http://hdl.handle.net/20.500.11769/16098 Zobrazit plný text záznamu