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Coen A. C. Ottenheijm et al.
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Identification of 45 novel mutations in the nebulin gene associated with autosomal recessive Nemaline myopathy
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Genotype-phenotype correlations in nemaline myopathy caused by mutations in the genes for nebulin and skeletal muscle α-actin
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Mutations in the nebulin gene can cause severe congenital nemaline myopathy
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Myopalladin, a novel 145-kilodalton sarcomeric protein with multiple roles in Z-disc and I-band protein assemblies
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