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Sarcomere dysfunction as the molecular basis of hypertrophic cardiomyopathy
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DOI：10.1038/s41569-026-01324-5.png)
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Abstract
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Dababneh and Roston describe the studies that first demonstrated that variants in genes encoding sarcomere proteins are the main cause of hypertrophic cardiomyopathy.
Journal
IF:
44.2
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289
Citations:
2.2W
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