Characterization of a novel, dominant negative KCNJ2 mutation associated with Andersen-Tawil syndrome.
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Bioelectric memory: modeling resting potential bistability in amphibian embryos and mammalian cellsGenome-wide analysis reveals conserved transcriptional responses downstream of resting potential change in Xenopus embryos, axolotl regeneration, and human mesenchymal cell differentiation.Genetically induced dysfunctions of Kir2.1 channels: implications for short QT3 syndrome and autism-epilepsy phenotype.
P2860
Characterization of a novel, dominant negative KCNJ2 mutation associated with Andersen-Tawil syndrome.
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2011 nî lūn-bûn
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2011年の論文
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2011年論文
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2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
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2011年论文
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2011年论文
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name
Characterization of a novel, d ...... with Andersen-Tawil syndrome.
@ast
Characterization of a novel, d ...... with Andersen-Tawil syndrome.
@en
type
label
Characterization of a novel, d ...... with Andersen-Tawil syndrome.
@ast
Characterization of a novel, d ...... with Andersen-Tawil syndrome.
@en
prefLabel
Characterization of a novel, d ...... with Andersen-Tawil syndrome.
@ast
Characterization of a novel, d ...... with Andersen-Tawil syndrome.
@en
P2093
P2860
P356
P1433
P1476
Characterization of a novel, d ...... with Andersen-Tawil syndrome.
@en
P2093
Jeanne M Nerbonne
Phillip S Cuculich
Scott B Marrus
P2860
P304
P356
10.4161/CHAN.5.6.18524
P577
2011-11-01T00:00:00Z