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Keyword [Ion channelopathy]
Result: 1 - 3 | Page: 1 of 1
1.
Genetic Research Of Disease-related Mutations And Clinical Study On Periodic Paralyses
2.
Genetic Research Of Ion Channel Gene Mutations And Clinical Study On Primary Hypokalemic Periodic Paralysis
3.
Mechanism Of A Novel Variant In SCN1B Linked To Brugada Syndrome And Construction Of Patient-sepcific Induced Pluripotent Stem Cells
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