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APA Citation
Du, F., Wang, G., Wang, D., Su, G., Yao, G., Zhang, W., & Su, G. (2020). targeted next generation sequencing revealed a novel deletion-frameshift mutation of KCNH2 gene in a Chinese Han family with long QT syndrome. Medicine, 99(16), . http://access.bl.uk/ark:/81055/vdc_100105908619.0x000039