Report of the 83rd ENMC International Workshop: 4th Workshop on Nemaline Myopathy, 22–24 September 2000, Naarden, The Netherlands

Author:

Wallgren-Pettersson Carina,Laing Nigel G

Publisher

Elsevier BV

Subject

Genetics(clinical),Clinical Neurology,Neurology,Pediatrics, Perinatology, and Child Health

Reference13 articles.

1. A novel nemaline myopathy in the Amish caused by a mutation in troponin T1;Johnston;Am J Hum Genet,2000

2. Mutations in the skeletal muscle alpha actin gene in patients with actin myopathy and nemaline myopathy;Nowak;Nat Genet,1999

3. Mutations in the beta-tropomyosin (TPM2) gene in rare cases of autosomal dominant nemaline myopathy. World Muscle Society Special Millennium Meeting, Kruger National Park, South Africa, 25–29 June, 2000;Donner;Neuromusc Disord,2000

4. Characterization of a novel cofilin isoform that is predominantly expressed in mammalian skeletal muscle;Ono;J Biol Chem,1994

5. Sequencing, expression analysis, and mapping of three unique human tropomodulin genes and their mouse orthologs;Cox;Genomics,2000

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