This is a preview of subscription content, access via your institution
Relevant articles
Open Access articles citing this article.
-
Clinically relevant intronic splicing enhancer mutation in myelin proteolipid protein leads to progressive microglia and astrocyte activation in white and gray matter regions of the brain
Journal of Neuroinflammation Open Access 05 December 2013
Access options
Subscribe to this journal
Receive 12 print issues and online access
$209.00 per year
only $17.42 per issue
Buy this article
- Purchase on Springer Link
- Instant access to full article PDF
Prices may be subject to local taxes which are calculated during checkout
References
Kenwrick, S. et al. Hum. Genet. 73, 264–266 (1986).
Keppen, L.D. et al. Am. J. hum. Genet. 41, 933–943 (1987).
Jouet, M. et al. Nature Genet. 7, 402–407 (1994).
Vits, L. et al. Nature Genet. 7, 408–413 (1994).
Johnston, A.W. & McKusick, V.A. Am. J. hum. Genet. 14, 83–94 (1962).
Ellis, D. & Malcolm, S. Nature Genet. 6, 333–334 (1994).
Aubourg, P. Nature Genet. 5, 105–106 (1993).
Saugier-Veber, P. et al. Nature Genet. 6, 257–262 (1994).
Schneider, A. et al. Nature 358, 758–761 (1992).
Griffiths, I.R. et al. J. Neurocytol. 19, 273–283 (1990).
Fanarraga, M. et al. Glia 5, 161–170 (1992).
Suter, U., Welcher, A.A. & Snipes, G.J. Trends Neurosci. 16, 50–56 (1993).
Readhead, C., Schneider, A., Griffiths, I. & Nave, K.-A. Neuron 12, 583–595 (1994).
Patel, P.I. & Lupski, J.R. Trends Genet. 10, 128–133 (1994).
Valentijn, L.J. et al. Nature Genet. 2, 288–291 (1992).
Strautnieks, S., Rutland, P., Winter, R.M., Baraitser, M. & Malcolm, S. Am. J. hum. Genet. 51, 871–878 (1992).
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Kobayashi, H., Hoffman, E. & Marks, H. The rumpshaker mutation in spastic paraplegia. Nat Genet 7, 351–352 (1994). https://doi.org/10.1038/ng0794-351
Issue Date:
DOI: https://doi.org/10.1038/ng0794-351
This article is cited by
-
Histological detection of dynamic glial responses in the dysmyelinating Tabby-jimpy mutant brain
Anatomical Science International (2018)
-
Clinically relevant intronic splicing enhancer mutation in myelin proteolipid protein leads to progressive microglia and astrocyte activation in white and gray matter regions of the brain
Journal of Neuroinflammation (2013)
-
Hereditary spastic paraplegia: clinico-pathologic features and emerging molecular mechanisms
Acta Neuropathologica (2013)
-
An autopsy case of adult-onset hereditary spastic paraplegia type 2 with a novel mutation in exon 7 of the proteolipid protein 1 gene
Acta Neuropathologica (2011)
-
Reevaluation of a large family defines a new locus for X-linked recessive pure spastic paraplegia (SPG34) on chromosome Xq25
neurogenetics (2008)