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03:45 min
August 08, 2022
DOI:
10.3791/63949-v
基于我们临床工作中发现的家族性遗传性心肌病家族,我们通过CRISPR / Cas9介导的基因组工程在小鼠MYH7位点创建了一个具有点突变(G823E)的C57BL / 6N小鼠模型来验证该突变。
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Xia, Y., Hu, J., Li, X., Zheng, S., Wang, G., Tan, S., Zou, Z., Ling, Q., Yang, F., Fan, X. Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model. J. Vis. Exp. (186), e63949, doi:10.3791/63949 (2022).
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