Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
8668742 | Journal of Electrocardiology | 2018 | 21 Pages |
Abstract
The DSG2 p.F531C was the main reason for ARVC/D. More severe phenotypes of ARVC/D occurred when coexisting with 217-1G>T or 524-3C>G mutation that potentially affecting the splicing function, as a compound heterozygous recessive inheritance.
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Authors
Yubi Lin, Jiana Huang, Ting Zhao, Siqi He, Zifeng Huang, Xiumin Chen, Hongwen Fei, Haiying Luo, Hui Liu, Shulin Wu, Xiufang Lin,