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A Korean Family of Hypokalemic Periodic Paralysis with Mutation in a Voltage-gated Calcium Channel (R1239G) 원문보기

Journal of Korean medical science : JKMS, v.20 no.1 = no.101, 2005년, pp.162 - 165  

Kim, June-Bum (Department of Pediatrics, College of Medicine, The Catholic University of Korea, Seoul, Korea.) ,  Lee, Kyung-Yil (Department of Pediatrics, College of Medicine, The Catholic University of Korea, Seoul, Korea.) ,  Hur, Jae-Kyun (Department of Pediatrics, College of Medicine, The Catholic University of Korea, Seoul, Korea.)

Abstract AI-Helper 아이콘AI-Helper

Hypokalemic periodic paralysis (HOPP) is a rare disease characterized by reversible attacks of muscle weakness accompanied by episodic hypokalemia. Recent molecular work has revealed that the majority of familial HOPP is due to mutations in a skeletal muscle voltage-dependent calcium-channel: the di...

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참고문헌 (28)

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