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

Journal article

Peer reviewed

P. Tan, J. Briner, E. Boltshauser, K. North, M.R. Davis, S.D. Wilton, C. Wallgren-Pettersson and N.G. Laing

Neuromuscular Disorders, Vol.7(6-7), pp.427-428

1997

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Title: Homozygosity for a nonsense mutation in the alpha-tropomyosin gene TPM3 in a patient with severe nemaline myopathy
Authors/Creators: P. Tan (Author/Creator)
J. Briner (Author/Creator)
E. Boltshauser (Author/Creator)
K. North (Author/Creator)
M.R. Davis (Author/Creator)
S.D. Wilton (Author/Creator) - Centre for Neuromuscular and Neurological Disorders
C. Wallgren-Pettersson (Author/Creator)
N.G. Laing (Author/Creator) - UWA Centre for Medical Research
Publication Details: Neuromuscular Disorders, Vol.7(6-7), pp.427-428
Publisher: Elsevier BV
Identifiers: 991005541448707891
Murdoch Affiliation: Murdoch University
Language: English
Resource Type: Journal article

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