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

P. Tan; J. Briner; E. Boltshauser; K. North; M.R. Davis; Steve Wilton; C. Wallgren-Pettersson; Nigel Laing

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

P. Tan, J. Briner, E. Boltshauser, K. North, M.R. Davis, Steve Wilton, C. Wallgren-Pettersson, Nigel Laing

Centre for Neuromuscular and Neurological Disorders (Perron Institute)
UWA Centre for Medical Research (affiliated with the Harry Perkins Institute of Medical Research)

Research output: Chapter in Book/Conference paper › Conference paper

Original language	English
Title of host publication	Second International Congress of the World Muscle Society
Editors	V. Dubowitz
Place of Publication	Great Britain
Publisher	Elsevier
Pages	427
Volume	7, Nos 6,7, September
Edition	Tunis, Tunisia
ISBN (Print)	09608966
Publication status	Published - 1997
Event	Homozygosity for a nonsense mutation in the alpha-tropomyosin gene TPM3 in a patient with severe nemaline myopathy - Tunis, Tunisia Duration: 1 Jan 1997 → …

Conference

Conference	Homozygosity for a nonsense mutation in the alpha-tropomyosin gene TPM3 in a patient with severe nemaline myopathy
Period	1/01/97 → …

Cite this

Tan, P., Briner, J., Boltshauser, E., North, K., Davis, M. R., Wilton, S., Wallgren-Pettersson, C., & Laing, N. (1997). Homozygosity for a nonsense mutation in the alpha-tropomyosin gene TPM3 in a patient with severe nemaline myopathy. In V. Dubowitz (Ed.), Second International Congress of the World Muscle Society (Tunis, Tunisia ed., Vol. 7, Nos 6,7, September, pp. 427). Elsevier.

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Tan, P, Briner, J, Boltshauser, E, North, K, Davis, MR, Wilton, S, Wallgren-Pettersson, C & Laing, N 1997, Homozygosity for a nonsense mutation in the alpha-tropomyosin gene TPM3 in a patient with severe nemaline myopathy. in V Dubowitz (ed.), Second International Congress of the World Muscle Society. Tunis, Tunisia edn, vol. 7, Nos 6,7, September, Elsevier, Great Britain, pp. 427, Homozygosity for a nonsense mutation in the alpha-tropomyosin gene TPM3 in a patient with severe nemaline myopathy, 1/01/97.

Homozygosity for a nonsense mutation in the alpha-tropomyosin gene TPM3 in a patient with severe nemaline myopathy. / Tan, P.; Briner, J.; Boltshauser, E. et al.

Second International Congress of the World Muscle Society. ed. / V. Dubowitz. Vol. 7, Nos 6,7, September Tunis, Tunisia. ed. Great Britain : Elsevier, 1997. p. 427.

Research output: Chapter in Book/Conference paper › Conference paper

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AU - Tan, P.

AU - Briner, J.

AU - Boltshauser, E.

AU - North, K.

AU - Davis, M.R.

AU - Wilton, Steve

AU - Wallgren-Pettersson, C.

AU - Laing, Nigel

PY - 1997

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SN - 09608966

VL - 7, Nos 6,7, September

SP - 427

BT - Second International Congress of the World Muscle Society

A2 - Dubowitz, V.

PB - Elsevier

CY - Great Britain

T2 - Homozygosity for a nonsense mutation in the alpha-tropomyosin gene TPM3 in a patient with severe nemaline myopathy

Y2 - 1 January 1997

ER -