Defining the disconnect between in vitro models and human arrhythmogenic disease: context matters.

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Analysis of SCN5A Gene Variants in East Slovak Patients with Cardiomyopathy.

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Defining the disconnect between in vitro models and human arrhythmogenic disease: context matters.

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2011 nî lūn-bûn

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Defining the disconnect betwee ...... enic disease: context matters.

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Defining the disconnect betwee ...... enic disease: context matters.

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Defining the disconnect betwee ...... enic disease: context matters.

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Defining the disconnect betwee ...... enic disease: context matters.

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Defining the disconnect betwee ...... enic disease: context matters.

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Defining the disconnect betwee ...... enic disease: context matters.

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Defining the disconnect betwee ...... enic disease: context matters.

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Amy C Sturm

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Peter J Mohler

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Spectrum and prevalence of mutations from the first 2,500 consecutive unrelated patients referred for the FAMILION long QT syndrome genetic test

SCN5A mutation associated with dilated cardiomyopathy, conduction disorder, and arrhythmia

Sodium channel mutations and susceptibility to heart failure and atrial fibrillation

A cardiac sodium channel mutation cosegregates with a rare connexin40 genotype in familial atrial standstill.

Active cascade screening in primary inherited arrhythmia syndromes: does it lead to prophylactic treatment?

Variable Na(v)1.5 protein expression from the wild-type allele correlates with the penetrance of cardiac conduction disease in the Scn5a(+/-) mouse model

Genotype-phenotype aspects of type 2 long QT syndrome.

A common single nucleotide polymorphism can exacerbate long-QT type 2 syndrome leading to sudden infant death.

Defining a new paradigm for human arrhythmia syndromes: phenotypic manifestations of gene mutations in ion channel- and transporter-associated proteins.

Striking In vivo phenotype of a disease-associated human SCN5A mutation producing minimal changes in vitro

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993-995

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scholarly article

editorial

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10.1161/CIRCULATIONAHA.111.051466

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English

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124

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2011-08-01T00:00:00Z

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51603855

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21875919

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3211044

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Defining the disconnect between in vitro models and human arrhythmogenic disease: context matters.

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Defining the disconnect between in vitro models and human arrhythmogenic disease: context matters.

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