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Your search keyword '"KCNJ2 mutation"' showing total 5 results

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Start Over You searched for: Descriptor "KCNJ2 mutation" Remove constraint Descriptor: "KCNJ2 mutation" Topic potassium channels, inwardly rectifying Remove constraint Topic: potassium channels, inwardly rectifying
5 results on '"KCNJ2 mutation"'

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1. Cardiac potassium inward rectifier Kir2: Review of structure, regulation, pharmacology, and arrhythmogenesis.

2. Characterization of a novel KCNJ2 sequence variant detected in Andersen-Tawil syndrome patients.

3. Identification and functional characterisation of a novel KCNJ2 mutation, Val302del, causing Andersen-Tawil syndrome.

4. Cardiac potassium inward rectifier Kir2: Review of structure, regulation, pharmacology, and arrhythmogenesis

5. Characterization of a novel KCNJ2 sequence variant detected in Andersen-Tawil syndrome patients

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