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 paperConference paper

Original languageEnglish
Title of host publicationSecond Asia-Pacific Conference on Medical Genetics and Eijkman Symposium on the Molecular Biology of Disease
Place of PublicationJakarta Indonesia
PublisherOrganising Committee. Second Asia-Pacific Conference on Medical Genetics and Eijkman Symposium on the Molecular Biology
Pages122
Volume1
Publication statusPublished - 1995
EventAn actin-binding site mutation in tropomyosin 3 causing autosomal dominant nemaline myopathy -
Duration: 1 Jan 1995 → …

Conference

ConferenceAn actin-binding site mutation in tropomyosin 3 causing autosomal dominant nemaline myopathy
Period1/01/95 → …

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