Novel CACNA1C R511Q mutation, located in domain - linker, causes non-syndromic type-8 long QT syndrome. Nakajima T, Kawabata-Iwakawa R, Tamura S, Hasegawa H, et al. PLoS One 2022;17:e0271796.

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Nakajima T, Kawabata-Iwakawa R, Tamura S, Hasegawa H, et al. Novel CACNA1C R511Q mutation, located in domain - linker, causes non-syndromic type-8 long QT syndrome. PLoS One 2022;17:e0271796.
PMID: 35862440