Research Article
Analysis of a Family with Brugada Syndrome and Sudden Cardiac Death Caused by a Novel Mutation of SCN5A
Table 1
Design of reverse transcription primers for qPCR detection of SCN5A in peripheral blood.
| Primer name | Primer sequence |
| SCN5A mutation site pre-qPCR F | 5′-CCAGACAGAGGGAGACTTGC-3′ | SCN5A mutation site pre-qPCR R | 3′-CTGGAGTCCACAGCTGCATA-5′ | qPCR after SCN5A mutation site F | 5′-CGCCTACGTGATGAGTGAGA-3′ | qPCR after SCN5A mutation site R | 3′-GTCGGCGAGATCTTCACTGT-5′ | hGAPDH F | 5′-CAAGGTCATCCATGACAACTTTG-3′ | hGAPDH R | 3′-GTCCACCACCCTGTTGCTGTAG-5′ |
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F as forward and R as reverse. |