Molecular diagnosis of hereditary inclusion body myopathy by linkage analysis and identification of a novel splice site mutation in GNE. (Q33943919)
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English | Molecular diagnosis of hereditary inclusion body myopathy by linkage analysis and identification of a novel splice site mutation in GNE. |
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Molecular diagnosis of hereditary inclusion body myopathy by linkage analysis and identification of a novel splice site mutation in GNE. (English)
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Steven E Boyden
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Anna R Duncan
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Elicia A Estrella
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Hart G W Lidov
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Lane J Mahoney
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Jonathan S Katz
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Louis M Kunkel
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Peter B Kang
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28 June 2011
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