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

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

S.D. Wilton, A. Akkari, S. Dorosz, K. Boundy and C. Kneebone
17th Annual Conference on the Organisation and Expression of the Genome (Erskine House, Lorne, Victoria, 13/02/1995–17/02/1995)
1995

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