- The Genotype and Clinical Phenotype of Korean Patients with Familial Hypokalemic Periodic Paralysis
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Kim JB, Kim MH, Lee SJ, Kim DJ, Lee BC
- KMID: 1785751
- J Korean Med Sci.
- 2007 Dec;22(6):946-951.
- doi: 10.3346/jkms.2007.22.6.946
Familial hypokalemic periodic paralysis (HOPP) is a rare autosomal-dominant disease characterized by reversible attacks of muscle weakness occurring with episodic hypokalemia. Mutations in the skeletal muscle calcium (CACNA1S) and sodium... -
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