Neuromuscular disorders

ISSNs: 0960-8966

Elsevier

Scopus rating (2021): CiteScore 5.8 SJR 0.98 SNIP 1.305

Journal

Publications

  1. 2010
  2. Fetal akinesia caused by a novel actin filament aggregate myopathy skeletal muscle actin gene (ACTA1) mutation

    Stenzel, W., Prokop, S., Kress, W., Huppmann, S., Loui, A., Sarioglu, N. M. E., Laing, N. G., Sparrow, J. C., Heppner, F. L. & Goebel, H. H., Aug 2010

    Article in Neuromuscular disorders

  3. Drosophila indirect flight muscle specific Act88F actin mutants as a model system for studying congenital myopathies of the human ACTA1 skeletal muscle actin gene

    Haigh, S. E., Salvi, S. S., Sevdali, M., Stark, M., Goulding, D., Clayton, J. D., Bullard, B., Sparrow, J. C. & Nongthomba, U., Jun 2010

    Article in Neuromuscular disorders

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