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Dive into the research topics of 'Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's syndrome'. Together they form a unique fingerprint.- Sort by
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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 Wolfe
Research output: Contribution to journal › Article › peer-review