PIP2 binding residues of Kir2.1 are common targets of mutations causing Andersen syndrome-Reference-Cited by-同舟云学术

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

Published:2003-06-10 Issue:11 Volume:60 Page:1811-1816
ISSN:0028-3878
Container-title:Neurology
language:en
Short-container-title:Neurology

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.,Ptacek L. J.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

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