Referenced in: none

Automatically associated channels: Kir2.1

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

Authors: N M Plaster, R Tawil, M Tristani-Firouzi, S Canún, S Bendahhou, A Tsunoda, M R Donaldson, S T Iannaccone, E Brunt, R Barohn, J Clark, F Deymeer, A L George, F A Fish, A Hahn, A Nitu, C Ozdemir, P Serdaroglu, S H Subramony, G Wolfe, Y H Fu, L J Ptácek

Journal, date & volume: Cell, 2001 May 18 , 105, 511-9

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/11371347

Abstract