A novel neuropsychiatric phenotype of KCNJ2 mutation in one Taiwanese family with Andersen-Tawil syndrome.
about
Potassium Channels and Human Epileptic Phenotypes: An Updated OverviewK(+) channelepsy: progress in the neurobiology of potassium channels and epilepsy.Biophysical and molecular characterization of a novel de novo KCNJ2 mutation associated with Andersen-Tawil syndrome and catecholaminergic polymorphic ventricular tachycardia mimicryNovel insights into the pathomechanisms of skeletal muscle channelopathies.Update on the implication of potassium channels in autism: K(+) channelautism spectrum disorder.Targets of polyamine dysregulation in major depression and suicide: Activity-dependent feedback, excitability, and neurotransmission.Genetically induced dysfunctions of Kir2.1 channels: implications for short QT3 syndrome and autism-epilepsy phenotype.Styrax blocks inward and outward current of Kir2.1 channel.
P2860
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P2860
A novel neuropsychiatric phenotype of KCNJ2 mutation in one Taiwanese family with Andersen-Tawil syndrome.
description
2010 nî lūn-bûn
@nan
2010年の論文
@ja
2010年学术文章
@wuu
2010年学术文章
@zh
2010年学术文章
@zh-cn
2010年学术文章
@zh-hans
2010年学术文章
@zh-my
2010年学术文章
@zh-sg
2010年學術文章
@yue
2010年學術文章
@zh-hant
name
A novel neuropsychiatric pheno ...... with Andersen-Tawil syndrome.
@en
A novel neuropsychiatric pheno ...... with Andersen-Tawil syndrome.
@nl
type
label
A novel neuropsychiatric pheno ...... with Andersen-Tawil syndrome.
@en
A novel neuropsychiatric pheno ...... with Andersen-Tawil syndrome.
@nl
prefLabel
A novel neuropsychiatric pheno ...... with Andersen-Tawil syndrome.
@en
A novel neuropsychiatric pheno ...... with Andersen-Tawil syndrome.
@nl
P2093
P50
P356
P1476
A novel neuropsychiatric pheno ...... with Andersen-Tawil syndrome.
@en
P2093
Hoi-Fong Chan
Jen-Jen Su
Li-Chin Ko
P2888
P304
P356
10.1038/JHG.2010.2
P577
2010-01-29T00:00:00Z
P5875
P6179
1024547032