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letter . 2004 Nov;41(11):842–848. doi: 10.1136/jmg.2004.020271
Missense mutations of ACTA1 cause dominant congenital myopathy with cores
A Kaindl
, F Ruschendorf
, S Krause
, H Goebel
, K Koehler
, C Becker
, D Pongratz
, J Muller-Hocker
, P Nurnberg
, G Stoltenburg-Didin
, H Lochmuller
, A Huebner
A Kaindl
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F Ruschendorf
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S Krause
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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 Muller-Hocker
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P Nurnberg
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G Stoltenburg-Didin
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H Lochmuller
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A Huebner
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PMCID: PMC1735626 PMID: 15520409