Mutations at the same amino acid in myosin that cause either skeletal or cardiac myopathy have distinct molecular phenotypes (Q33787873)
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English | Mutations at the same amino acid in myosin that cause either skeletal or cardiac myopathy have distinct molecular phenotypes |
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Mutations at the same amino acid in myosin that cause either skeletal or cardiac myopathy have distinct molecular phenotypes (English)
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Thomas Z Armel
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Leslie A Leinwand
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23 October 2009
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48
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1007-1013
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