Variants of the elongator protein 3 (ELP3) gene are associated with motor neuron degeneration

Amyotrophic lateral sclerosis (ALS) is a spontaneous, relentlessly progressive motor neuron disease, usually resulting in death from respiratory failure within 3 years. Variation in the genes SOD1 and TARDBP accounts for a small percentage of cases, and other genes have shown association in both can...

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Detalles Bibliográficos
Autores principales: Simpson, Claire L., Lemmens, Robin, Miskiewicz, Katarzyna, Broom, Wendy J., Hansen, Valerie K., van Vught, Paul W.J., Landers, John E., Sapp, Peter, Van Den Bosch, Ludo, Knight, Joanne, Neale, Benjamin M., Turner, Martin R., Veldink, Jan H., Ophoff, Roel A., Tripathi, Vineeta B., Beleza, Ana, Shah, Meera N., Proitsi, Petroula, Van Hoecke, Annelies, Carmeliet, Peter, Horvitz, H. Robert, Leigh, P. Nigel, Shaw, Christopher E., van den Berg, Leonard H., Sham, Pak C., Powell, John F., Verstreken, Patrik, Brown, Robert H., Robberecht, Wim, Al-Chalabi, Ammar
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2009
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2638803/
https://www.ncbi.nlm.nih.gov/pubmed/18996918
http://dx.doi.org/10.1093/hmg/ddn375

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2638803/
https://www.ncbi.nlm.nih.gov/pubmed/18996918
http://dx.doi.org/10.1093/hmg/ddn375

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