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Impaired neurotransmission in ether lipid-deficient nerve terminals

Isolated defects of ether lipid (EL) biosynthesis in humans cause rhizomelic chondrodysplasia punctata type 2 and type 3, serious peroxisomal disorders. Using a

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Bibliographic Details
Main Authors: Brodde, Alexander (Author) , Teigler, André (Author) , Brügger, Britta (Author) , Lehmann, Wolf-Dieter (Author) , Wieland, Felix T. (Author) , Just, Wilhelm W. (Author)
Format: Article (Journal)
Language:English
Published: 08 March 2012
In: Human molecular genetics
Year: 2012, Volume: 21, Issue: 12, Pages: 2713-2724
ISSN:1460-2083
DOI:10.1093/hmg/dds097
Online Access:Verlag, kostenfrei, Volltext: http://dx.doi.org/10.1093/hmg/dds097
Verlag, kostenfrei, Volltext: https://academic.oup.com/hmg/article/21/12/2713/2900659
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Author Notes:Alexander Brodde, Andre Teigler, Britta Brugger, Wolf D. Lehmann, Felix Wieland, Johannes Berger and Wilhelm W. Just
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Summary:Isolated defects of ether lipid (EL) biosynthesis in humans cause rhizomelic chondrodysplasia punctata type 2 and type 3, serious peroxisomal disorders. Using a
Item Description:Gesehen am 06.08.2018
Physical Description:Online Resource
ISSN:1460-2083
DOI:10.1093/hmg/dds097

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