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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. Wilton, A. Akkari, K. Boundy, C. Kneebone, P. Blumberg, S. White, H. Watkins, D. Love and N.G. Laing
Second Asia-Pacific Conference on Medical Genetics and Eijkman Symposium on the Molecular Biology of Disease (Shangri-La Hotel, Jakarta, Indonesia, 19/09/1995–23/09/1995)
1995

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