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

By Klebe Stephan  

Neurogenetics, Vol. 8, Iss. 2, 2007-04 ,pp. : 155-157

Springer Publishing Company

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A novel mutation in the SPG3A gene (atlastin) in hereditary spastic paraplegia

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Journal of Neurology, Vol. 254, Iss. 7, 2007-07 ,pp. : 972-974

Springer Publishing Company

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A clinical, genetic and biochemical study of SPG7 mutations in hereditary spastic paraplegia

By Wilkinson P.A.   Crosby A.H.   Turner C.   Bradley L.J.   Ginsberg L.   Wood N.W.   Schapira A.H.   Warner T.T.  

Brain, Vol. 127, Iss. 9, 2004-09 ,pp. : 2148-2148

Oxford University Press

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A clinical, genetic and biochemical study of SPG7 mutations in hereditary spastic paraplegia

By Wilkinson Philip A.  

Brain, Vol. 127, Iss. 5, 2004-05 ,pp. : 973-980

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

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Neurogenetics, Vol. 5, Iss. 1, 2004-02 ,pp. : 49-54

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