Population
51 Korean patients from 20 families diagnosed with familial hypokalemic periodic paralysis (HOPP)
Design
Cohort
Authors
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Mutation status may guide prognostic counseling in Korean hypokalemic periodic paralysis; leaves open whether genotyping alters management.
The study provides comprehensive genotype-phenotype data for Korean patients with familial hypokalemic periodic paralysis, highlighting the predominance of the CACNA1S Arg528His mutation and distinct clinical features based on mutation status.
Kim et al. (2007) studied this question.
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