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Homozygosity for a nonsense mutation in the alpha-tropomyosin gene TPM3 in a patient with severe nemaline myopathy

Tan, P., Briner, J., Boltshauser, E., North, K., Davis, M.R., Wilton, S.D., Wallgren-Pettersson, C. and Laing, N.G. (1997) Homozygosity for a nonsense mutation in the alpha-tropomyosin gene TPM3 in a patient with severe nemaline myopathy. Neuromuscular Disorders, 7 (6-7). pp. 427-428.

Link to Published Version: http://dx.doi.org/10.1016/S0960-8966(97)87165-9
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Abstract

No abstract available

Item Type: Journal Article
Publisher: Elsevier BV
Copyright: © 1997 Elsevier B.V.
URI: http://researchrepository.murdoch.edu.au/id/eprint/21750
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