(Q37749844)

22 August 2017

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title

Genetic basis of malignant channelopathies and ventricular fibrillation in the structurally normal heart (English)

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22 August 2017

main subject

ventricular fibrillation

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Arthur A M Wilde

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22 August 2017

Nynke Hofman

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22 August 2017

Laura T van Lochem

series ordinal

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22 August 2017

language of work or name

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1 May 2010

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22 August 2017

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22 August 2017

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22 August 2017

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22 August 2017

page(s)

395-408

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Task Force on Sudden Cardiac Death of the European Society of Cardiology.

22 August 2017

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Arrhythmogenic mutation-linked defects in ryanodine receptor autoregulation reveal a novel mechanism of Ca2+ release channel dysfunction

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

1 reference

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21 January 2018

1 reference

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21 January 2018

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Identification of a possible pathogenic link between congenital long QT syndrome and epilepsy

21 January 2018

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SCN5A is expressed in human jejunal circular smooth muscle cells

21 January 2018

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Sodium channel mutation in irritable bowel syndrome: evidence for an ion channelopathy

21 January 2018

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A novel early onset lethal form of catecholaminergic polymorphic ventricular tachycardia maps to chromosome 7p14-p22

21 January 2018

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Congenital long QT syndrome

21 January 2018

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21 January 2018

Identifiers

DOI

10.2217/FCA.10.11

1 reference

22 August 2017

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