The prevalent I686T human variant and loss of function...

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The prevalent I686T human variant and loss of function mutations in the cardiomyocyte-specific kinase gene TNNI3K cause adverse contractility and concentric remodeling in mice

Gan, Peiheng, Baicu, Catalin, Watanabe, Hirofumi, Wang, Kristy, Tao, Ge, Judge, Daniel P, Zile, Michael R, Makita, Takako, Mukherjee, Rupak, Sucov, Henry M
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Journal:
Human Molecular Genetics
DOI:
10.1093/hmg/ddaa234
Date:
October, 2020
File:
PDF, 1013 KB
2020
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