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Tnni3k alleles influence ventricular mononuclear diploid cardiomyocyte frequency.
PLoS Genet. 2019 Oct 7;15(10):e1008354. doi: 10.1371/journal.pgen.1008354. eCollection 2019 Oct.
PLoS Genet. 2019.
PMID: 31589606
Free PMC article.
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 P, Baicu C, Watanabe H, Wang K, Tao G, Judge DP, Zile MR, Makita T, Mukherjee R, Sucov HM.
Gan P, et al.
Hum Mol Genet. 2021 Jan 6;29(21):3504-3515. doi: 10.1093/hmg/ddaa234.
Hum Mol Genet. 2021.
PMID: 33084860
Free PMC article.
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