161st ENMC International Workshop on nemaline myopathy and related disorders, Newcastle upon Tyne, 2008
Author:
Publisher
Elsevier BV
Subject
Genetics(clinical),Clinical Neurology,Neurology,Pediatrics, Perinatology, and Child Health
Reference25 articles.
1. Mutations in TPM3 are a common cause of congenital fiber type disproportion;Clarke;Ann Neurol,2008
2. Nemaline myopathy with minicores caused by mutation of the CFL2 gene encoding the skeletal muscle actin-binding protein, cofilin-2;Agrawal;Am J Hum Genet,2007
3. Sporadic late-onset nemaline myopathy effectively treated by melphalan and stem cell transplant;Voermans;Neurology,2008
4. Stem cell transplantation in a patient with late-onset nemaline myopathy and gammopathy;Benveniste;Neurology,2008
5. A “nema” of hope in the treatment of late-onset nemaline myopathy;Dalakas;Neurology,2008
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