Original language | English |
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Pages (from-to) | 31-36 |
Journal | Neuromuscular Disorders |
Volume | 21 |
DOIs | |
Publication status | Published - 2011 |
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 journal › Review article
22
Citations
(Scopus)