Congenital disorders of autophagy: an emerging novel class of inborn errors of neuro-metabolism

Mutations in autophagy genes cause childhood-onset multisystem diseases with predominant nervous system involvement and provide a ‘genetic window’ into autophag

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Bibliographic Details
Main Authors:	Ebrahimi-Fakhari, Darius (Author) , Saffari, Afshin (Author) , Wahlster, Lara (Author) , Lu, Jenny (Author) , Byrne, Susan (Author) , Hoffmann, Georg F. (Author) , Jungbluth, Heinz (Author) , Sahin, Mustafa (Author)
Format:	Article (Journal)
Language:	English
Published:	2016
In:	Brain Year: 2015, Volume: 139, Issue: 2, Pages: 317-337
ISSN:	1460-2156
DOI:	10.1093/brain/awv371
Online Access:	Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1093/brain/awv371 Verlag, lizenzpflichtig, Volltext: https://academic.oup.com/brain/article/139/2/317/1754062
Author Notes:	Darius Ebrahimi-Fakhari, Afshin Saffari, Lara Wahlster, Jenny Lu, Susan Byrne, Georg F. Hoffmann, Heinz Jungbluth and Mustafa Sahin

Description
Summary:	Mutations in autophagy genes cause childhood-onset multisystem diseases with predominant nervous system involvement and provide a ‘genetic window’ into autophag
Item Description:	Advance access publication December 29, 2015 Gesehen am 04.05.2020
Physical Description:	Online Resource
ISSN:	1460-2156
DOI:	10.1093/brain/awv371