Inherited disorders of the neuromuscular junction: an update
Author:
Publisher
Springer Science and Business Media LLC
Subject
Neurology (clinical),Neurology
Link
http://link.springer.com/content/pdf/10.1007/s00415-014-7520-7.pdf
Reference83 articles.
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3. Senderek J, Müller JS, Dusl M et al (2011) Hexosamine biosynthetic pathway mutations cause neuromuscular transmission defect. Am J Hum Genet 88:162–172
4. Cossins J, Belaya K, Hicks D et al (2013) Congenital myasthenic syndromes due to mutations in ALG2 and ALG14. Brain 136:944–956
5. Chaouch A, Beeson D, Hantaï D, Lochmüller H (2012) 186th ENMC international workshop: congenital myasthenic syndromes 24–26 June 2011, Naarden, The Netherlands. Neuromuscul Disord 22:566–576
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