Related content

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

By Bot Susanne   Vermeer Sascha   Buijsman Wendy   Heister Angelien   Voorendt Marsha   Verrips Aad   Scheffer Hans   Kremer Hubertus   Warrenburg Bart   Kamsteeg Erik-Jan  

Journal of Neurology, Vol. 260, Iss. 7, 2013-07 ,pp. : 1765-1769

Springer Publishing Company

Access to resources Recommend Favorite

A novel mutation in the HSPD1 gene in a patient with hereditary spastic paraplegia

By Hansen J.   Svenstrup K.   Ang D.   Nielsen M.   Christensen J.   Gregersen N.   Nielsen J.   Georgopoulos C.   Bross P.  

Journal of Neurology, Vol. 254, Iss. 7, 2007-07 ,pp. : 897-900

Springer Publishing Company

Access to resources Recommend Favorite

A novel mutation in KIF5A gene causing hereditary spastic paraplegia with axonal neuropathy

By Musumeci Olimpia  

Neurological Sciences, Vol. 32, Iss. 4, 2011-08 ,pp. : 665-668

Springer Publishing Company

Access to resources Recommend Favorite

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

Access to resources Recommend Favorite

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

Oxford University Press

Access to resources Recommend Favorite