Severe nemaline myopathy caused by mutations of the stop codon of the skeletal muscle alpha actin gene (ACTA1).
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| Description | scientific article published on September 2006 |
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author: Rita Horvath Ichizo Nishino Hanns Lochmüller Nigel G Laing Zoltán Molnár Danielle E. Dye |
| Publication date | September 1, 2006 |
| Language | English |
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