Fig. 2
From: Genetic analysis of 37 cases with primary periodic paralysis in Chinese patients
Pedigree and genetic analysis of five patients with primary periodic paralysis. (A) Patient 17, CACNA1S c.3716G > A mutation. (B) Patient 5, SCN4A c.2111 C > T (p.T704M) mutation. (C) Patient 8, SCN4A c.2015G > A (p.R675Q) mutation. (D) Patient 2, SCN4A c.2024G > A mutation (E) Patient 7, SCN4A c.4774 A > G mutation