Title : Lack of any cardiac involvement in a patient with Andersen-Tawil syndrome associated with the c.574A→G mutation in KCNJ2.

Pub. Date : 2011

PMID : 22286118






2 Functional Relationships(s)
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Compound Name
Protein Name
Organism
1 Most cases are caused by mutations in KCNJ2, encoding for the potassium inwardly rectifying channel, Kir2.1 (ATS1). Potassium potassium inwardly rectifying channel subfamily J member 2 Homo sapiens
2 Most cases are caused by mutations in KCNJ2, encoding for the potassium inwardly rectifying channel, Kir2.1 (ATS1). Potassium potassium inwardly rectifying channel subfamily J member 2 Homo sapiens