Mutations in Potassium Channel Kir2.6 Cause Susceptibility to Thyrotoxic Hypokalemic Periodic Paralysis-Reference-Cited by-同舟云学术

Mutations in Potassium Channel Kir2.6 Cause Susceptibility to Thyrotoxic Hypokalemic Periodic Paralysis

Published:2010-01 Issue:1 Volume:140 Page:88-98
ISSN:0092-8674
Container-title:Cell
language:en
Short-container-title:Cell

Author:

Ryan Devon P.,Dias da Silva Magnus R.,Soong Tuck Wah,Fontaine Bertrand,Donaldson Matt R.,Kung Annie W.C.,Jongjaroenprasert Wallaya,Liang Mui Cheng,Khoo Daphne H.C.,Cheah Jin Seng,Ho Su Chin,Bernstein Harold S.,Maciel Rui M.B.,Brown Robert H.,Ptáček Louis J.

Publisher

Elsevier BV

Subject

General Biochemistry, Genetics and Molecular Biology

Reference35 articles.

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4. A novel sodium channel mutation in a family with hypokalemic periodic paralysis;Bulman;Neurology,1999

5. PIP2 binding residues of Kir2.1 are common targets of mutations causing Andersen syndrome;Donaldson;Neurology,2003

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