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

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. ; Kneebone, C. ; Blumberg, P. ; White, S. ; Watkins, H. ; Love, D. ; Laing, Nigel. / 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

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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",

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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.; Kneebone, C.; Blumberg, P.; White, S.; Watkins, H.; Love, D.; Laing, Nigel.

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