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An actin-binding site mutation in tropomyosin 3 causing autosomal dominant nemaline myopathy

Wilton, S., Akkari, A., Boundy, K., Kneebone, C., Blumberg, P., White, S., Watkins, H., Love, D. and Laing, N.G. (1995) An actin-binding site mutation in tropomyosin 3 causing autosomal dominant nemaline myopathy. In: Second Asia-Pacific Conference on Medical Genetics and Eijkman Symposium on the Molecular Biology of Disease, 19 - 23 September 1995, Shangri-La Hotel, Jakarta, Indonesia.

Abstract

No abstract available

Publication Type: Conference Item
URI: http://researchrepository.murdoch.edu.au/id/eprint/21915
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