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  Genetic dissection of oligodendroglial and neuronal Plp1 function in a novel mouse model of spastic paraplegia type 2

Lüders, K. A., Patzig, J., Simons, M., Nave, K.-A., & Werner, H. B. (2017). Genetic dissection of oligodendroglial and neuronal Plp1 function in a novel mouse model of spastic paraplegia type 2. Glia, 65(11), 1762-1776. doi:10.1002/glia.23193.

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Item Permalink: https://hdl.handle.net/11858/00-001M-0000-002E-2A72-4 Version Permalink: https://hdl.handle.net/21.11116/0000-000D-3089-2
Genre: Journal Article

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Lueders_17.pdf (Publisher version), 2MB
 
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 Creators:
Lüders, Katja A.1, Author           
Patzig, Julia1, Author           
Simons, Mikael2, Author           
Nave, Klaus-Armin1, Author           
Werner, Hauke B.1, Author           
Affiliations:
1Neurogenetics, Max Planck Institute of Experimental Medicine, Max Planck Society, ou_2173664              
2Cellular neuroscience, Max Planck Institute of Experimental Medicine, Max Planck Society, ou_2173650              

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Free keywords: Oligodendrocyte; Myelin; Neurodegeneration; Neuroinflammation; Proteolipid protein (PLP); FA2H; GJC2/CX47; Hereditary spastic paraplegia type 2 (SPG2); Glia-axonal support; Axonopathy
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Language(s): eng - English
 Dates: 2017-06-292017-08-242017-11
 Publication Status: Issued
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 Rev. Type: Peer
 Identifiers: DOI: 10.1002/glia.23193
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Title: Glia
Source Genre: Journal
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Publ. Info: New York, N.Y. : Wiley-Liss, Inc.
Pages: - Volume / Issue: 65 (11) Sequence Number: - Start / End Page: 1762 - 1776 Identifier: ISSN: 0894-1491
CoNE: https://pure.mpg.de/cone/journals/resource/954925558509