A New Cardiac Channelopathy: From Clinical Phenotypes to Molecular Mechanisms Associated With Na1.5 Gating Pores

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A New Cardiac Channelopathy: From Clinical Phenotypes to Molecular Mechanisms Associated With Na1.5 Gating Pores

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наукова стаття, опублікована у 2018

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A New Cardiac Channelopathy: F ...... ciated With Na1.5 Gating Pores

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A New Cardiac Channelopathy: F ...... ciated With Na1.5 Gating Pores

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A New Cardiac Channelopathy: F ...... ciated With Na1.5 Gating Pores

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A New Cardiac Channelopathy: F ...... ciated With Na1.5 Gating Pores

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A New Cardiac Channelopathy: F ...... ciated With Na1.5 Gating Pores

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A New Cardiac Channelopathy: F ...... ciated With Na1.5 Gating Pores

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P1476

A New Cardiac Channelopathy: F ...... ciated With Na1.5 Gating Pores

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P2093

Adrien Moreau

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Mohamed Chahine

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P2860

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Primary structure and functional expression of the human cardiac tetrodotoxin-insensitive voltage-dependent sodium channel

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A Gating Charge Transfer Center in Voltage Sensors

A single Na(+) channel mutation causing both long-QT and Brugada syndromes

From ionic currents to molecular mechanisms: the structure and function of voltage-gated sodium channels

Spectrum of mutations in long-QT syndrome genes. KVLQT1, HERG, SCN5A, KCNE1, and KCNE2

Congenital sick sinus syndrome caused by recessive mutations in the cardiac sodium channel gene (SCN5A)

Genetic basis and molecular mechanism for idiopathic ventricular fibrillation

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139

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scholarly article

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10.3389/FCVM.2018.00139

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English

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2018-01-01T00:00:00Z

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30356750

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6189448

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