Mutations in FUS cause FALS and SALS in French and French Canadian populations

Background: The identification of mutations in the TARDBP and more recently the identification of mutations in the FUS gene as the cause of amyotrophic lateral sclerosis (ALS) is providing the field with new insight about the mechanisms involved in this severe neurodegenerative disease. Methods: To...

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Autores principales: Belzil, V. V., Valdmanis, P. N., Dion, P. A., Daoud, H., Kabashi, E., Noreau, A., Gauthier, J., Hince, P., Desjarlais, A., Bouchard, J. -P., Lacomblez, L., Salachas, F., Pradat, P. -F., Camu, W., Meininger, V., Dupré, N., Rouleau, G. A.
Formato: Artigo
Lenguaje:Inglês
Publicado: Lippincott Williams & Wilkins 2009
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Articles
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC3462471/
https://ncbi.nlm.nih.gov/pubmed/19741216
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/WNL.0b013e3181bbfeef
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