Age-related axonal and myelin changes in the rumpshaker mutation of the Plp gene

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Expression of a Myelin Proteolipid Protein (Plp)-lacZ Transgene is Reduced in both the CNS and PNS of Plp ^jp Mice

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NIPA1 ( SPG6 ) mutations are a rare cause of autosomal dominant spastic paraplegia in Europe

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Narrowing of the critical region in autosomal recessive spastic paraplegia linked to the SPG5 locus

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Pure adult-onset Spastic Paraplegia caused by a novel mutation in the KIAA0196 (SPG8) gene

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