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

Wilton, S.D., Akkari, A., Dorosz, S., Boundy, K. and Kneebone, C. (1995) An actin-binding site mutation in tropomyosin 3 causing autosomal dominant nemaline myopathy. In: 17th Annual Conference on the Organisation and Expression of the Genome, 13 - 17 February 1995, Erskine House, Lorne, Victoria.

Abstract

No abstract available

Publication Type: Conference Item
URI: http://researchrepository.murdoch.edu.au/id/eprint/21936
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