An actin-binding site mutation in tropomyosin 3 causing autosomal dominant nemaline myopathy

Steve Wilton; Anthony Akkari; K. Boundy; C. Kneebone; P. Blumberg; S. White; H. Watkins; D. Love; Nigel Laing

An actin-binding site mutation in tropomyosin 3 causing autosomal dominant nemaline myopathy

Steve Wilton, Anthony Akkari, K. Boundy, C. Kneebone, P. Blumberg, S. White, H. Watkins, D. Love, 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 Asia-Pacific Conference on Medical Genetics and Eijkman Symposium on the Molecular Biology of Disease
Place of Publication	Jakarta Indonesia
Publisher	Organising Committee. Second Asia-Pacific Conference on Medical Genetics and Eijkman Symposium on the Molecular Biology
Pages	122
Volume	1
Publication status	Published - 1995
Event	An actin-binding site mutation in tropomyosin 3 causing autosomal dominant nemaline myopathy - Duration: 1 Jan 1995 → …

Conference

Conference	An actin-binding site mutation in tropomyosin 3 causing autosomal dominant nemaline myopathy
Period	1/01/95 → …

Cite this

Wilton, S., Akkari, A., Boundy, K., Kneebone, C., Blumberg, P., White, S., Watkins, H., Love, D., & Laing, N. (1995). An actin-binding site mutation in tropomyosin 3 causing autosomal dominant nemaline myopathy. In Second Asia-Pacific Conference on Medical Genetics and Eijkman Symposium on the Molecular Biology of Disease (Vol. 1, pp. 122). Organising Committee. Second Asia-Pacific Conference on Medical Genetics and Eijkman Symposium on the Molecular Biology.

Wilton, Steve ; Akkari, Anthony ; Boundy, K. et al. / An actin-binding site mutation in tropomyosin 3 causing autosomal dominant nemaline myopathy. Second Asia-Pacific Conference on Medical Genetics and Eijkman Symposium on the Molecular Biology of Disease. Vol. 1 Jakarta Indonesia : Organising Committee. Second Asia-Pacific Conference on Medical Genetics and Eijkman Symposium on the Molecular Biology, 1995. pp. 122

@inproceedings{8912a28997394e7fa3307af9c1c026d5,

title = "An actin-binding site mutation in tropomyosin 3 causing autosomal dominant nemaline myopathy",

author = "Steve Wilton and Anthony Akkari and K. Boundy and C. Kneebone and P. Blumberg and S. White and H. Watkins and D. Love and Nigel Laing",

year = "1995",

language = "English",

volume = "1",

pages = "122",

booktitle = "Second Asia-Pacific Conference on Medical Genetics and Eijkman Symposium on the Molecular Biology of Disease",

publisher = "Organising Committee. Second Asia-Pacific Conference on Medical Genetics and Eijkman Symposium on the Molecular Biology",

note = "An actin-binding site mutation in tropomyosin 3 causing autosomal dominant nemaline myopathy ; Conference date: 01-01-1995",

}

Wilton, S , Akkari, A, Boundy, K, Kneebone, C, Blumberg, P, White, S, Watkins, H, Love, D & Laing, N 1995, An actin-binding site mutation in tropomyosin 3 causing autosomal dominant nemaline myopathy. in Second Asia-Pacific Conference on Medical Genetics and Eijkman Symposium on the Molecular Biology of Disease. vol. 1, Organising Committee. Second Asia-Pacific Conference on Medical Genetics and Eijkman Symposium on the Molecular Biology, Jakarta Indonesia, pp. 122, An actin-binding site mutation in tropomyosin 3 causing autosomal dominant nemaline myopathy, 1/01/95.

An actin-binding site mutation in tropomyosin 3 causing autosomal dominant nemaline myopathy. / Wilton, Steve ; Akkari, Anthony; Boundy, K. et al.
Second Asia-Pacific Conference on Medical Genetics and Eijkman Symposium on the Molecular Biology of Disease. Vol. 1 Jakarta Indonesia: Organising Committee. Second Asia-Pacific Conference on Medical Genetics and Eijkman Symposium on the Molecular Biology, 1995. p. 122.

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

TY - GEN

T1 - An actin-binding site mutation in tropomyosin 3 causing autosomal dominant nemaline myopathy

AU - Wilton, Steve

AU - Akkari, Anthony

AU - Boundy, K.

AU - Kneebone, C.

AU - Blumberg, P.

AU - White, S.

AU - Watkins, H.

AU - Love, D.

AU - Laing, Nigel

PY - 1995

Y1 - 1995

M3 - Conference paper

VL - 1

SP - 122

BT - Second Asia-Pacific Conference on Medical Genetics and Eijkman Symposium on the Molecular Biology of Disease

PB - Organising Committee. Second Asia-Pacific Conference on Medical Genetics and Eijkman Symposium on the Molecular Biology

CY - Jakarta Indonesia

T2 - An actin-binding site mutation in tropomyosin 3 causing autosomal dominant nemaline myopathy

Y2 - 1 January 1995

ER -

Wilton S , Akkari A, Boundy K, Kneebone C, Blumberg P, White S et al. An actin-binding site mutation in tropomyosin 3 causing autosomal dominant nemaline myopathy. In Second Asia-Pacific Conference on Medical Genetics and Eijkman Symposium on the Molecular Biology of Disease. Vol. 1. Jakarta Indonesia: Organising Committee. Second Asia-Pacific Conference on Medical Genetics and Eijkman Symposium on the Molecular Biology. 1995. p. 122