Ion channel gene expression predicts survival in glioma patients
Author:
Publisher
Springer Science and Business Media LLC
Subject
Multidisciplinary
Link
http://www.nature.com/articles/srep11593.pdf
Reference60 articles.
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3. Yang, N. et al. Sodium channel mutations in paramyotonia congenita exhibit similar biophysical phenotypes in vitro. Proc. Natl. Acad. Sci. U S A 91, 12785–12789 (1994).
4. Zerr, P., Adelman, J. P. & Maylie, J. Episodic ataxia mutations in Kv1.1 alter potassium channel function by dominant negative effects or haploinsufficiency. J. Neurosci. 18, 2842–2848 (1998).
5. Carrera, P., Stenirri, S., Ferrari, M. & Battistini, S. Familial hemiplegic migraine: a ion channel disorder. Brain Res. Bull. 56, 239–241 (2001).
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