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...

詳細記述

保存先:
書誌詳細
主要な著者: 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.
フォーマット: Artigo
言語:Inglês
出版事項: Lippincott Williams & Wilkins 2009
主題:
Articles
オンライン･アクセス: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
タグ: タグ追加
タグなし, このレコードへの初めてのタグを付けませんか!

類似資料