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PIP2 binding residues of Kir2.1 are common targets of mutations causing Andersen syndrome.

Document Type

journal article

Author

Donaldson, M R; Jensen, J L; Tristani-Firouzi, M; Tawil, R; Bendahhou, S; Suarez, W A; Cobo, A M; Poza, J J; Behr, E; Wagstaff, J; Szepetowski, P; Pereira, S; Mozaffar, T; Escolar, D M; Fu, Y-H; Ptácek, L J

Source

Neurology; 2003 Jun 10, Vol. 60 Issue 11, p1811-1816, 6p

Subject

Language

ISSN

00283878

Online Access

Full Text (LWW Journals - Ovid) Full Text (LWW total - Ovid) Full Text (LWW Premier Journals) Web of Science JCR 저널정보 Scopus Find it@PNU

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