A novel ACTA1 mutation resulting in a severe congenital myopathy with nemaline bodies, intranuclear rods and type I fibre predominance (Q39654455)
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scientific article published on 17 September 2010
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English | A novel ACTA1 mutation resulting in a severe congenital myopathy with nemaline bodies, intranuclear rods and type I fibre predominance |
scientific article published on 17 September 2010 |
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A novel ACTA1 mutation resulting in a severe congenital myopathy with nemaline bodies, intranuclear rods and type I fibre predominance (English)
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Gianina Ravenscroft
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Komala Pillay
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Padma Sivadorai
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William Wallefeld
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Kristen J Nowak
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17 September 2010
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21
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1
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31-36
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