CACNA1C mutations are present in a small percentage (2.2%) of Japanese patients with inherited arrhythmias, presenting with varied phenotypes and highlighting the potential clinical importance of LTCC gene screening.
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May warrant CACNA1C inclusion in Japanese arrhythmia panels; leaves open sex-specific penetrance and ECG overlap with SCN5A.
Fukuyama et al. (2013) studied this question.
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