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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Rare Diseases

Last data update: Jan 25, 2025. (Total: 235671Documents)
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Query Trace: Familial Periodic Paralysis[original query]
Skeletal muscle dihydropyridine-sensitive calcium channel (CACNA1S) gene mutations in chinese patients with hypokalemic periodic paralysis.
The American journal of the medical sciences 2005 Feb 329 (2): 66-70.
Lin Shih-Hua, Hsu Yaw-Don, Cheng Nai-Lin, Kao Ming-Chi
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