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Homozygous alpha-tropomyosin (TMP3) nonsense mutation in fatal congenital nemaline myopathy

Tan, P., Briner, J., Boltshauser, E., Davis, M.R., Wilton, S.D., Wallgren-Pettersson, C. and Laing, N.G. (1997) Homozygous alpha-tropomyosin (TMP3) nonsense mutation in fatal congenital nemaline myopathy. In: Human Genetics Society of Australasia. 21st Annual Scientific Meeting. Human Genetics: Diversity and Disease, 21 - 25 July 1997, Perth, Western Australia.

Abstract

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Publication Type: Conference Item
Conference Website: http://www.hgsa.org.au/
URI: http://researchrepository.murdoch.edu.au/id/eprint/21922
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