A troponin T mutation that causes infantile restrictive cardiomyopathy increases Ca2+ sensitivity of force development and impairs the inhibitory properties of troponin (Q24301265)
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scientific article
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | A troponin T mutation that causes infantile restrictive cardiomyopathy increases Ca2+ sensitivity of force development and impairs the inhibitory properties of troponin |
scientific article |
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A troponin T mutation that causes infantile restrictive cardiomyopathy increases Ca2+ sensitivity of force development and impairs the inhibitory properties of troponin (English)
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25 January 2008
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283
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4
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2156-66
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