Centronuclear Myopathies
Author:
Publisher
Elsevier BV
Subject
Clinical Neurology,Pediatrics, Perinatology, and Child Health
Reference39 articles.
1. Congenital myopathies;Fardeau,1994
2. A gene mutated in X-linked myotubular myopathy defines a new putative tyrosine phosphatase family conserved in yeast;Laporte;Nat Genet,1996
3. Clinical and histologic findings in autosomal centronuclear myopathy;Jeannet;Neurology,2004
4. Mutations in dynamin 2 cause dominant centronuclear myopathy;Bitoun;Nat Genet,2005
5. Mutations in amphiphysin 2 (BIN1) disrupt interaction with dynamin 2 and cause autosomal recessive centronuclear myopathy;Nicot;Nat Genet,2007
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