Fig. 3From: A novel CACNA1S gene variant in a child with hypokalemic periodic paralysis: a case report and literature reviewPhenotype-genotype comparison by types of CACNA1S gene variants. Truncated variants are grouped in a unique category; missense variants are grouped by localization of the amino-acid substitution. HypoPP: hypokalemic periodic paralysis; MHS: malignant hyperthermia susceptibility; CM: congenital myopathy; TM: transmembraneBack to article page