Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's syndrome by Plaster N M, Tawil R, Tristani-Firouzi M, Canún S, Bendahhou S, Tsunoda A, Donaldson M R, Iannaccone S T, Brunt E, Barohn R, Clark J, Deymeer F, George A L, Fish F A, Hahn A, Nitu A, Ozdemir C, Serdaroglu P, Subramony S H, Wolfe G, Fu Y H, Ptácek L J in Cell (2001).

[PMID: 11371347] PubMed


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