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          Institute: MPI für experimentelle Medizin     Collection: Neurogenetics     Display Documents



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ID: 434725.0, MPI für experimentelle Medizin / Neurogenetics
Different proteolipid protein mutants exhibit unique metabolic defects
Authors:Hüttemann, Maik; Zhang, Zhan; Mullins, Chadwick; Bessert, Denise; Lee, Icksoo; Nave, Klaus-Armin; Appikatla, Sunita; Skoff, Robert P.
Language:English
Date of Publication (YYYY-MM-DD):2009-08-07
Title of Journal:ASN NEURO
Sequence Number of Article:AN20090028
Review Status:Peer-review
Audience:Experts Only
Free Keywords:Mitochondria; Oligodendrocytes; Oxidative phosphorylation; Pelizaeus-Merzbacher disease; Plp1 mutants
External Publication Status:published
Document Type:Article
Version Comment:Automatic journal name synchronization
Communicated by:Klaus-Armin Nave
Affiliations:MPI für experimentelle Medizin/Neurogenetics
External Affiliations:Departement of Anatomy and Cell Biology, Center for Molecular Medicine and Genetics, Wayne State University School of Medicine, Detroit, MI
Identifiers:DOI:10.1042/AN20090028
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