Current status of the congenital myasthenic syndromes
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health
Reference112 articles.
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4. Mutations in LAMB2 causing a severe form of synaptic congenital myasthenic syndrome;Maselli;J Med Genet,2009
5. Sporadic centronuclear myopathy with muscle pseudohypertrophy, neutropenia, and necklace fibers due to a DNM2 mutation;Liewluck;Neuromuscul Disord,2010
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