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Characterization of kinesin switch I mutations that cause hereditary spastic paraplegia
Kif5A is a neuronally-enriched isoform of the Kinesin-1 family of cellular transport motors. 23 separate mutations in the motor domain of Kif5A have been identified in patients with the complicated form of hereditary spastic paraplegia (HSP). We performed in vitro assays on dimeric recombinant Kif5A...
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| Publicado no: | PLoS One |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Public Library of Science
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5498027/ https://ncbi.nlm.nih.gov/pubmed/28678816 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0180353 |
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