Andersen's syndrome mutants produce a knockdown of inwardly rectifying K+ channel in mouse skeletal muscle in vivo.

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Andersen's syndrome mutants produce a knockdown of inwardly rectifying K+ channel in mouse skeletal muscle in vivo.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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Andersen's syndrome mutants pr ...... mouse skeletal muscle in vivo.

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Andersen's syndrome mutants pr ...... mouse skeletal muscle in vivo.

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Andersen's syndrome mutants pr ...... mouse skeletal muscle in vivo.

@en

Andersen's syndrome mutants pr ...... mouse skeletal muscle in vivo.

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Andersen's syndrome mutants pr ...... mouse skeletal muscle in vivo.

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Andersen's syndrome mutants pr ...... mouse skeletal muscle in vivo.

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P1476

Andersen's syndrome mutants pr ...... mouse skeletal muscle in vivo

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P2093

Ana Vukolic

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Bruno Allard

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Gaëlle Robin

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Kay-Dietrich Wagner

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Nicolas Guy

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Pamela Moceri

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Saïd Bendahhou

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Serena Giuliano

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P2860

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Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's syndrome

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A novel form of short QT syndrome (SQT3) is caused by a mutation in the KCNJ2 gene

Molecular cloning and expression of a human heart inward rectifier potassium channel

Cloning and functional characterization of a novel ATP-sensitive potassium channel ubiquitously expressed in rat tissues, including pancreatic islets, pituitary, skeletal muscle, and heart

Characterization and variation of a human inwardly-rectifying-K-channel gene (KCNJ6): a putative ATP-sensitive K-channel subunit

Functional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome)

Human G-protein-coupled inwardly rectifying potassium channel (GIRK1) gene (KCNJ3): localization to chromosome 2 and identification of a simple tandem repeat polymorphism

P2888

s00441-017-2696-7

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309-323

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P31

scholarly article

P356

10.1007/S00441-017-2696-7

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P433

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P478

371

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Dina Simkin

Alain Lacampagne

P577

2017-10-10T00:00:00Z

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P698

29018970

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