Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's syndrome

Nikki M. Plaster, Rabi Tawil, Martin Tristani-Firouzi, Sonia Canún, Sad Bendahhou, Akiko Tsunoda, Matthew R. Donaldson, Susan T. Iannaccone, Ewout Brunt, Richard Barohn, John Clark, Feza Deymeer, Alfred L. George, Frank A. Fish, Angelika Hahn, Alexandru Nitu, Coskun Ozdemir, Piraye Serdaroglu, S. H. Subramony, Gil WolfeYing Hui Fu, Louis J. Ptáček*

*Corresponding author for this work

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