Mouse Models for Thin Filament Disease
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Publisher
Springer New York
Link
http://link.springer.com/content/pdf/10.1007/978-0-387-84847-1_6.pdf
Reference68 articles.
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2. Wallefeld W, Krause S, Nowak KJ et al. Severe nemaline myopathy caused by mutations of the stop codon of skeletal muscle alpha actin gene (ACTA1). Neuromuscul Disord 2006; 16:541–547.
3. D’Amico A, Graziano C, Pacileo G et al. Fatal hypertrophic cardiomyopathy and nemaline myopathy associated with ACTA1 K336E mutation. Neuro muscul Disord 2006; 16:548–552.
4. Nowak KJ, Sewry CA, Navarro C et al. Nemaline myopathy caused by absence of alpha-skeletal muscle actin. Ann Neurol 2007; 61(2):175–184.
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1. Case report: A novel ACTA1 variant in a patient with nemaline rods and increased glycogen deposition;Frontiers in Neurology;2024-03-04
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