A mutation in the a tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathy

Nigel Laing, Steve Wilton, P.A. Akkari, S. Dorosz, K. Boundy, C. Kneebone, P. Blumbergs, S. White, H. Watkins, D.R. Love, E. Haan

Research output: Contribution to journalArticlepeer-review

58 Citations (Web of Science)
Original languageEnglish
Pages (from-to)75-79
JournalNature Genetics
Issue numberJanuary
Publication statusPublished - 1995

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