Case ReportPublished 12 October 2026KCNJ2 gene spontaneous missense mutation in a child with Andersen-Tawil syndrome: a case reportMeiqi Feng · Xi Wang · Lingshan Hu · Lei ZhangFrontiers in Pediatricsdoi 10.3389/fped.2026.1961456
Original ResearchPublished 8 January 2026Functional study of a novel SCN4A variant c.611C>T identified in a Japanese patient with myastheniaNatsuki Kira · Kosuke Yoshida · Satoe Takahashi · Ayami Yamanaka · Takashi Kimura · Kazuaki Homma · Masanori P. Takahashi · Tomoya KubotaFrontiers in Biophysicsdoi 10.3389/frbis.2025.1710099
