Congenital Myasthenic Syndromes in 2012
Author:
Publisher
Springer Science and Business Media LLC
Subject
Neurology (clinical),General Neuroscience
Link
http://link.springer.com/content/pdf/10.1007/s11910-011-0234-7.pdf
Reference67 articles.
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3. Tsujino A, Maertens C, Ohno K, et al. Myasthenic syndrome caused by mutation of the SCN4A sodium channel. Proc Natl Acad Sci USA. 2003;100:7377–82.
4. Engel AG, Ohno K, Wang H-L, et al. Molecular basis of congenital myasthenic syndromes: Mutations in the acetylcholine receptor. Neuroscientist. 1998;4:185–94.
5. Ohno K, Brengman JM, Tsujino A, Engel AG. Human endplate acetylcholinesterase deficiency caused by mutations in the collagen-like tail subunit (ColQ) of the asymmetric enzyme. Proc Natl Acad Sci USA. 1998;95:9654–9.
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