109th ENMC International Workshop: 5th Workshop on nemaline myopathy, 11th–13th October 2002, Naarden, The Netherlands
- 1 August 2003
- journal article
- review article
- Published by Elsevier in Neuromuscular Disorders
- Vol. 13 (6) , 501-507
- https://doi.org/10.1016/s0960-8966(03)00007-5
Abstract
No abstract availableThis publication has 10 references indexed in Scilit:
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- A mutation in alpha-tropomyosinslow affects muscle strength, maturation and hypertrophy in a mouse model for nemaline myopathyHuman Molecular Genetics, 2001
- An autosomal dominant congenital myopathy with cores and rods is associated with a neomutation in the RYR1 gene encoding the skeletal muscle ryanodine receptorHuman Molecular Genetics, 2000
- Report of the 70th ENMC International Workshop: Nemaline myopathy, 11–13 June 1999, Naarden, The NetherlandsNeuromuscular Disorders, 2000
- Clinical and genetic heterogeneity in autosomal recessive nemaline myopathyNeuromuscular Disorders, 1999