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Homozygosity for a nonsense mutation in the alpha-tropomyosin gene TPM3 in a patient with fatal, congenital, nemaline myopathy with intranuclear rods

Tan, P., Briner, J., Boltshauser, E., Davis, M.R., Wilton, S.D., Wallgren-Pettersson, C. and Laing, N.G. (1996) Homozygosity for a nonsense mutation in the alpha-tropomyosin gene TPM3 in a patient with fatal, congenital, nemaline myopathy with intranuclear rods. In: 7th Annual Combined Biological Sciences Meeting, 19 August 1996, Perth, Western Australia.

Abstract

No abstract available

Item Type: Conference Item
URI: http://researchrepository.murdoch.edu.au/id/eprint/21928
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