The spectrum of KIAA0196 variants, and characterization of a murine knockout: implications for the mutational mechanism in hereditary spastic paraplegia type SPG8

BACKGROUND: The hereditary spastic paraplegias (HSPs) are rare neurodegenerative gait disorders which are genetically highly heterogeneous. For each single form, eventual consideration of therapeutic strategies requires an understanding of the mechanism by which mutations confer pathogenicity. SPG8...

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Detalles Bibliográficos
Autores principales: Jahic, Amir, Khundadze, Mukhran, Jaenisch, Nadine, Schüle, Rebecca, Klimpe, Sven, Klebe, Stephan, Frahm, Christiane, Kassubek, Jan, Stevanin, Giovanni, Schöls, Ludger, Brice, Alexis, Hübner, Christian A., Beetz, Christian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4647479/
https://www.ncbi.nlm.nih.gov/pubmed/26572744
http://dx.doi.org/10.1186/s13023-015-0359-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4647479/
https://www.ncbi.nlm.nih.gov/pubmed/26572744
http://dx.doi.org/10.1186/s13023-015-0359-x

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