A novel ACTA1 mutation resulting in a severe congenital myopathy with nemaline bodies, intranuclear rods and type I fibre predominance

Gina Ravenscroft, J.M. Wilmshurst, K. Pillay, P. Sivadori, William Wallefeld, Kristen Nowak, Nigel Laing

Research output: Contribution to journalReview article

22 Citations (Scopus)
Original languageEnglish
Pages (from-to)31-36
JournalNeuromuscular Disorders
Volume21
DOIs
Publication statusPublished - 2011

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