Targeted disruption of the Mast syndrome gene SPG21 in mice impairs hind limb function and alters axon branching in cultured cortical neurons-Reference-Cited by-同舟云学术

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Targeted disruption of the Mast syndrome gene SPG21 in mice impairs hind limb function and alters axon branching in cultured cortical neurons

Published:2010-07-27 Issue:4 Volume:11 Page:369-378
ISSN:1364-6745
Container-title:neurogenetics
language:en
Short-container-title:Neurogenetics

Author:

Soderblom Cynthia,Stadler Julia,Jupille Henri,Blackstone Craig,Shupliakov Oleg,Hanna Michael C.

Publisher

Springer Science and Business Media LLC

Subject

Cellular and Molecular Neuroscience,Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s10048-010-0252-7.pdf

Reference30 articles.

1. Harding AE (1983) Classification of the hereditary ataxias and paraplegias. Lancet 1:1151–1155

2. Salinas S, Proukakis C, Crosby A, Warner TT (2008) Hereditary spastic paraplegia: clinical features and pathogenetic mechanisms. Lancet Neurol 7:1127–1138

3. Reid E (2003) Science in motion: common molecular pathological themes emerge in the hereditary spastic paraplegias. J Med Genet 40:81–86

4. Fink JK (2006) Hereditary spastic paraplegia. Curr Neurol Neurosci Rep 6:65–76

5. Soderblom C, Blackstone C (2006) Traffic accidents: molecular genetic insights into the pathogenesis of the hereditary spastic paraplegias. Pharmacol Ther 109:42–56

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