Article

Idetification of <i>CACNA1B</i> (p.K567R) mutation responsible for familiar AVNRT

2022-03-10

Abstract excerpt

Atrioventricular nodal reentry tachycardia (AVNRT) is the most common form of paroxysmal supraventricular tachycardia (PSVT). The exact cause of AVNRT has not yet been found. However, an increasing number of reports suggest that AVNRT is hereditary, but no precise pathogenic gene has been found so far. In our study, we found that a point mutation of CACNA1B (p.K567R) which encoded the α1 subunit of N-type calcium...

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Literature Corpus work: 80bde6ea-c93c-5560-a82d-e0debea6d87e
DOI: 10.1101/2022.03.09.22271906

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