Author:
Zang Lili,Wang Jingmin,Jiang Yuwu,Gu Qiang,Gao Zhijie,Yang Yanling,Xiao Jiangxi,Wu Ye
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Reference34 articles.
1. Li, R., Jonhson, A. B., Salomons, G., Goldman, J. E., Naidu, S., Quinlan, R. & Wu, Y. Glial fibrillary acidic protein mutations in infantile, juvenile, and adult forms of Alexander disease. Ann. Neurol. 57, 310–326 (2005).
2. Johnson, A. B. & Brenner, M. Alexander disease: a review and the gene. Int. J. Dev. Neurosci. 20, 391–394 (2002).
3. Prust, M., Wang, J., Morizono, H., Messing, A., Brenner, M., Gordon, E. et al. GFAP mutations, age at onset, and clinical subtypes in Alexander disease. Neurology 77, 1287–1294 (2011).
4. Johnson, A. B. & Bettica, A. On-grid immunogold labeling of glial intermediate filaments in epoxy-embedded tissue. Am. J. Anat. 185, 335–341 (1989).
5. Head, M. W., Corbin, E. & Goldman, J. E. Overexpression and abnormal modification of the stress proteins alpha B-crystallin and HSP27 in Alexander disease. Am. J. Pathol. 143, 1743–1753 (1993).
Cited by
16 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献