Dynamin 2 mutations in Charcot-Marie-Tooth neuropathy highlight the importance of clathrin-mediated endocytosis in myelination

Abstract. Mutations in dynamin 2 (DNM2) lead to dominant intermediate Charcot-Marie-Tooth neuropathy type B, while a different set of DNM2 mutations cause auto

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Bibliographic Details
Main Authors: Sidiropoulos, Páris (Author) , Kuner, Rohini (Author)
Format: Article (Journal)
Language:English
Published: March 26, 2012
In: Brain
Year: 2012, Volume: 135, Issue: 5, Pages: 1395-1411
ISSN:1460-2156
DOI:10.1093/brain/aws061
Online Access:Verlag, Volltext: http://dx.doi.org/10.1093/brain/aws061
Verlag, Volltext: https://academic.oup.com/brain/article/135/5/1395/306911
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Author Notes:Páris N. M. Sidiropoulos, Michaela Miehe, Thomas Bock, Elisa Tinelli, Carole I. Oertli, Rohini Kuner, Dies Meijer, Bernd Wollscheid, Axel Niemann and Ueli Suter
Description
Summary:Abstract. Mutations in dynamin 2 (DNM2) lead to dominant intermediate Charcot-Marie-Tooth neuropathy type B, while a different set of DNM2 mutations cause auto
Item Description:Advance access publication March 26, 2012
Gesehen am 13.08.2018
Physical Description:Online Resource
ISSN:1460-2156
DOI:10.1093/brain/aws061