A mutation in the KCNE3 potassium channel gene is associated with susceptibility to thyrotoxic hypokalemic periodic paralysis
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Deep resequencing of the voltage-gated potassium channel subunit KCNE3 gene in chronic tinnitusDisruption of the K+ channel beta-subunit KCNE3 reveals an important role in intestinal and tracheal Cl- transportKCNE beta subunits determine pH sensitivity of KCNQ1 potassium channelsWorking model for the structural basis for KCNE1 modulation of the KCNQ1 potassium channel.Analytic review: thyrotoxic periodic paralysis: a review.Thyrotoxic periodic paralysis: an overview.The KCNE genes in hypertrophic cardiomyopathy: a candidate gene study.A young man presenting with paralysis after vigorous exercise.The primary periodic paralyses: diagnosis, pathogenesis and treatment.Hypokalemic periodic paralysis: a model for a clinical and research approach to a rare disorder.Neuromuscular complications of thyrotoxicosis.KCNE1 and KCNE3: The yin and yang of voltage-gated K(+) channel regulationIon channelopathies in endocrinology: recent genetic findings and pathophysiological insights.Novel etiopathophysiological aspects of thyrotoxic periodic paralysis.Thyrotoxic periodic paralysis: clinical and molecular aspects.Thyrotoxic Periodic Paralysis and Polymorphisms of the ADRB2, AR, and GABRA3 Genes in Men with Graves DiseaseAn unusual cause of muscle weakness: a diagnostic challenge for clinicians.Molecular cloning of ion channels in Felis catus that are related to periodic paralyses in man: a contribution to the understanding of the genetic susceptibility to feline neck ventroflexion and paralysis.Concurrence of thyrotoxicosis and Gitelman's syndrome-associated hypokalemia-induced periodic paralysis.Manifestation, management and molecular analysis of candidate genes in two rare cases of thyrotoxic hypokalemic periodic paralysis.Association of genetic variants in GABRA3 gene and thyrotoxic hypokalaemic periodic paralysis in Thai population.No mutation in the KCNE3 potassium channel gene in Chinese thyrotoxic hypokalaemic periodic paralysis patients.[Thyrotoxic hypokalemic periodic paralysis, an endocrine emergency: clinical and genetic features in 25 patients].Thyrotoxic periodic paralysis associated with a mutation in the sodium channel gene SCN4A.Arg16Gly polymorphism in beta2-adrenergic receptor gene is not associated with thyrotoxic periodic paralysis in Korean male patients with Graves' disease
P2860
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P2860
A mutation in the KCNE3 potassium channel gene is associated with susceptibility to thyrotoxic hypokalemic periodic paralysis
description
2002 nî lūn-bûn
@nan
2002 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
name
A mutation in the KCNE3 potass ...... hypokalemic periodic paralysis
@ast
A mutation in the KCNE3 potass ...... hypokalemic periodic paralysis
@en
A mutation in the KCNE3 potass ...... hypokalemic periodic paralysis
@nl
type
label
A mutation in the KCNE3 potass ...... hypokalemic periodic paralysis
@ast
A mutation in the KCNE3 potass ...... hypokalemic periodic paralysis
@en
A mutation in the KCNE3 potass ...... hypokalemic periodic paralysis
@nl
prefLabel
A mutation in the KCNE3 potass ...... hypokalemic periodic paralysis
@ast
A mutation in the KCNE3 potass ...... hypokalemic periodic paralysis
@en
A mutation in the KCNE3 potass ...... hypokalemic periodic paralysis
@nl
P2093
P356
P1476
A mutation in the KCNE3 potass ...... hypokalemic periodic paralysis
@en
P2093
Janete M Cerutti
Liliane A T Arnaldi
Magnus R Dias Da Silva
Rui M B Maciel
P304
P356
10.1210/JC.2002-020698
P407
P577
2002-11-01T00:00:00Z