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

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

ISSN： 0340-5354

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

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Related content

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

By Matsui M. Kawarai T. Hase Y. Tomimoto H. Iseki K. Rogaeva E. Orlacchio A. Bernardi G. George-Hyslop P. Takahashi R. Matsui M.

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

Springer Publishing Company

Access to resources Recommend Favorite

Novel mutation in the SPAST gene in a patient with spastic paraparesis

By Vergouwen M. Sistermans E. Baas F. Koelman J. Visser M.

Journal of Neurology, Vol. 255, Iss. 2, 2008-02 ,pp. : 303-304

Springer Publishing Company

Access to resources Recommend Favorite

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 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

Enhanced reticulospinal output in patients with (REEP1) hereditary spastic paraplegia type 31

By Fisher K. Chinnery P. Baker S. Baker M.

Journal of Neurology, Vol. 260, Iss. 12, 2013-12 ,pp. : 3182-3184

Springer Publishing Company

Access to resources Recommend Favorite