An actin-binding site mutation in tropomyosin 3 causing autosomal dominant nemaline myopathy
S. Wilton, A. Akkari, K. Boundy, C. Kneebone, P. Blumberg, S. White, H. Watkins, D. Love and N.G. Laing
Second Asia-Pacific Conference on Medical Genetics and Eijkman Symposium on the Molecular Biology of Disease (Shangri-La Hotel, Jakarta, Indonesia, 19/09/1995–23/09/1995)
1995
Abstract
No abstract available
Details
Title
An actin-binding site mutation in tropomyosin 3 causing autosomal dominant nemaline myopathy
Authors/Creators
S. Wilton (Author/Creator)
A. Akkari (Author/Creator)
K. Boundy (Author/Creator)
C. Kneebone (Author/Creator)
P. Blumberg (Author/Creator)
S. White (Author/Creator)
H. Watkins (Author/Creator)
D. Love (Author/Creator)
N.G. Laing (Author/Creator)
Conference
Second Asia-Pacific Conference on Medical Genetics and Eijkman Symposium on the Molecular Biology of Disease (Shangri-La Hotel, Jakarta, Indonesia, 19/09/1995–23/09/1995)