Gene dosage-dependent rescue of HSP neurite defects in SPG4 patients' neurons-Reference-Cited by-同舟云学术

Gene dosage-dependent rescue of HSP neurite defects in SPG4 patients' neurons

Published:2013-12-30 Issue:10 Volume:23 Page:2527-2541
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Human Molecular Genetics

Author:

Havlicek S.,Kohl Z.,Mishra H. K.,Prots I.,Eberhardt E.,Denguir N.,Wend H.,Plotz S.,Boyer L.,Marchetto M. C. N.,Aigner S.,Sticht H.,Groemer T. W.,Hehr U.,Lampert A.,Schlotzer-Schrehardt U.,Winkler J.,Gage F. H.,Winner B.

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/23/10/2527/1689105/ddt644.pdf

Reference35 articles.

1. Erratum: Hereditary spastic paraplegias: membrane traffic and the motor pathway

2. Direct evidence for axonal transport defects in a novel mouse model of mutant spastin-induced hereditary spastic paraplegia (HSP) and human HSP patients

3. Hereditary spastic paraparesis: Disrupted intracellular transport associated with spastin mutation

4. The Cellular and Molecular Pathology of the Motor System in Hereditary Spastic Paraparesis due to Mutation of the Spastin Gene

5. Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia

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