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Mutations in the skeletal muscle α-actin gene in patients with actin myopathy and nemaline myopathy.
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A common nonsense mutation results in α-actinin-3 deficiency in the general population.
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NEW PERSPECTIVES IN PEDIATRIC NEUROMUSCULAR DISORDERS Hotel Intercontinental Sydney, Sydney, Australia, August 28, 1998.
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Abnormalities of dystrophin, the sarcoglycans, and laminin alpha2 in the muscular dystrophies..
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