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Orphanet Journal of Rare Diseases|October 28, 2022
Whole exome sequencing in Brugada and long QT syndromes revealed novel rare and potential pathogenic mutations related to the dysfunction of the cardiac sodium channelJia Chen, Hong Li, Sicheng Guo, et al.
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Showing results (31-40 of 31) with videos related to

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You have reached the last page of results.This site can display upto 31 results.
Orphanet Journal of Rare Diseases|October 28, 2022
Whole exome sequencing in Brugada and long QT syndromes revealed novel rare and potential pathogenic mutations related to the dysfunction of the cardiac sodium channelJia Chen, Hong Li, Sicheng Guo, et al.
Pageof 4