Enhanced myosin function due to a point mutation causing a familial hypertrophic cardiomyopathy (Q33891494)
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English | Enhanced myosin function due to a point mutation causing a familial hypertrophic cardiomyopathy |
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Enhanced myosin function due to a point mutation causing a familial hypertrophic cardiomyopathy (English)
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Moss RL
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Periera JS
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1 April 2000
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86
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720-722
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Identifiers
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