(Q24676050)

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Missense mutations of ACTA1 cause dominant congenital myopathy with cores

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Missense mutations of ACTA1 cause dominant congenital myopathy with cores (English)
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A M Kaindl
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F Rüschendorf
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S Krause
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H-H Goebel
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K Koehler
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C Becker
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D Pongratz
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J Müller-Höcker
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P Nürnberg
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G Stoltenburg-Didinger
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A Huebner
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November 2004
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41
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11
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842-8
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