A Kinesin Heavy Chain (KIF5A) Mutation in Hereditary Spastic Paraplegia (SPG10)
- 1 November 2002
- journal article
- Published by Elsevier BV in American Journal of Human Genetics
- Vol. 71 (5), 1189-1194
- https://doi.org/10.1086/344210
Abstract
No abstract availableKeywords
This publication has 25 references indexed in Scilit:
- SPG20 is mutated in Troyer syndrome, an hereditary spastic paraplegiaNature Genetics, 2002
- Hereditary spastic paraplegia: The pace quickensAnnals of Neurology, 2002
- Hereditary spastic paraparesis: a review of new developmentsJournal of Neurology, Neurosurgery & Psychiatry, 2000
- Microtubule-Based Transport Systems in Neurons: The Roles of Kinesins and DyneinsAnnual Review of Neuroscience, 2000
- A New Locus for Autosomal Dominant “Pure” Hereditary Spastic Paraplegia Mapping to Chromosome 12q13, and Evidence for Further Genetic HeterogeneityAmerican Journal of Human Genetics, 1999
- Chromosomal Localization Reveals Three Kinesin Heavy Chain Genes in MouseGenomics, 1998
- CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choiceNucleic Acids Research, 1994
- Cloning by insertional mutagenesis of a cDNA encoding Caenorhabditis elegans kinesin heavy chain.Proceedings of the National Academy of Sciences of the United States of America, 1993
- Kinesin-related gene unc-104 is required for axonal transport of synaptic vesicles in C. elegansCell, 1991
- Kinesin heavy chain is essential for viability and neuromuscular functions in Drosophila, but mutants show no defects in mitosisCell, 1991