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    Genetic Background Influences UPR but not PLP Processing in the rumpshaker Model of PMD/SPG2

    Mutations of the proteolipid protein gene (PLP1) cause Pelizaeus-Merzbacher disease (PMD) and Spastic paraplegia type 2 (SPG2). The rumpshaker mutation is associated with mild forms of PMD or SPG2 in man and the ...

    M. McLaughlin, S. A. Karim, P. Montague, J. A. Barrie, D. Kirkham… in Neurochemical Research (2007)