Statistics for K7del is a common TPM2 gene mutation associated with nemaline myopathy and raised myofibre calcium sensitivity
Total visits
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K7del is a common TPM2 gene mutation associated with nemaline myopathy and raised myofibre calcium sensitivity | 659 |
Total visits per month
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June 2024 | 0 |
July 2024 | 0 |
August 2024 | 0 |
September 2024 | 0 |
October 2024 | 0 |
November 2024 | 0 |
December 2024 | 0 |
Top country views
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Russia | 6 |
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Japan | 5 |
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Canada | 2 |
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Greece | 1 |
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