SCN3B:NaV1.5

Sahib S Sarbjit-Singh1, Samir W Hamaia1, Christopher A Beaudoin1

  • 1Department of Biochemistry, University of Cambridge, Tennis Court Road, Cambridge CB2 1QW, UK.

概括

一种新型的SCN3B基因缺失导致布鲁加达综合征 (BrS) 通过损害心脏通道功能,尽管结构变化最小. 这一发现揭示了NaV1.5通道调节和心脏刺激性的复杂性.

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