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publicationName Journal of molecular and cellular cardiology
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bibliographicCitation Armel TZ, Leinwand LA. Mutations at the same amino acid in myosin that cause either skeletal or cardiac myopathy have distinct molecular phenotypes. Journal of Molecular and Cellular Cardiology. 2010 May;48(5):1007–13. doi: 10.1016/j.yjmcc.2009.10.011.
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https://doi.org/10.1016/j.yjmcc.2009.10.011
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language English
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title Mutations at the same amino acid in myosin that cause either skeletal or cardiac myopathy have distinct molecular phenotypes
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Total number of triples: 39.