(Q34263609)

1 August 2017

1 reference

title

Genetic aspects of arrhythmias (English)

1 reference

1 August 2017

2

Brugada R

1 reference

1 August 2017

Roberts R

1

1 reference

1 August 2017

1 January 2000

1 reference

American Journal of Medical Genetics Part A

1 August 2017

1 reference

1 August 2017

97

1 reference

1 August 2017

310-318

1 reference

1 August 2017

4

1 reference

MiRP1 forms IKr potassium channels with HERG and is associated with cardiac arrhythmia

1 August 2017

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200024%2997%3A4%3C310%3A%3AAID-AJMG1282%3E3.0.CO%3B2-7

Localization of a gene responsible for arrhythmogenic right ventricular dysplasia to chromosome 3p23.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200024%2997%3A4%3C310%3A%3AAID-AJMG1282%3E3.0.CO%3B2-7

Cardiac involvement in mitochondrial diseases. A study on 17 patients with documented mitochondrial DNA defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200024%2997%3A4%3C310%3A%3AAID-AJMG1282%3E3.0.CO%3B2-7

Familial atrial standstill with coexistent atrial flutter

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200024%2997%3A4%3C310%3A%3AAID-AJMG1282%3E3.0.CO%3B2-7

K(V)LQT1 and lsK (minK) proteins associate to form the I(Ks) cardiac potassium current

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200024%2997%3A4%3C310%3A%3AAID-AJMG1282%3E3.0.CO%3B2-7

High resolution fluorescence in situ hybridization to linearly extended DNA visually maps a tandem repeat associated with facioscapulohumeral muscular dystrophy immediately adjacent to the telomere of 4q.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200024%2997%3A4%3C310%3A%3AAID-AJMG1282%3E3.0.CO%3B2-7

A novel X-linked gene, G4.5. is responsible for Barth syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200024%2997%3A4%3C310%3A%3AAID-AJMG1282%3E3.0.CO%3B2-7

Identification of a novel X-linked gene responsible for Emery-Dreifuss muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200024%2997%3A4%3C310%3A%3AAID-AJMG1282%3E3.0.CO%3B2-7

Cardiac myosin binding protein-C gene splice acceptor site mutation is associated with familial hypertrophic cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200024%2997%3A4%3C310%3A%3AAID-AJMG1282%3E3.0.CO%3B2-7

Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200024%2997%3A4%3C310%3A%3AAID-AJMG1282%3E3.0.CO%3B2-7

Right bundle branch block, persistent ST segment elevation and sudden cardiac death: A distinct clinical and electrocardiographic syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200024%2997%3A4%3C310%3A%3AAID-AJMG1282%3E3.0.CO%3B2-7

Sodium channel blockers identify risk for sudden death in patients with ST-segment elevation and right bundle branch block but structurally normal hearts

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200024%2997%3A4%3C310%3A%3AAID-AJMG1282%3E3.0.CO%3B2-7

Right bundle-branch block and ST-segment elevation in leads V1 through V3: a marker for sudden death in patients without demonstrable structural heart disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200024%2997%3A4%3C310%3A%3AAID-AJMG1282%3E3.0.CO%3B2-7

Identification of a genetic locus for familial atrial fibrillation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200024%2997%3A4%3C310%3A%3AAID-AJMG1282%3E3.0.CO%3B2-7

Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200024%2997%3A4%3C310%3A%3AAID-AJMG1282%3E3.0.CO%3B2-7

Absence of myotonic dystrophy protein kinase (DMPK) mRNA as a result of a triplet repeat expansion in myotonic dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200024%2997%3A4%3C310%3A%3AAID-AJMG1282%3E3.0.CO%3B2-7

Cardiomyopathy in the Kearns-Sayre syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200024%2997%3A4%3C310%3A%3AAID-AJMG1282%3E3.0.CO%3B2-7

Genetic basis and molecular mechanism for idiopathic ventricular fibrillation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200024%2997%3A4%3C310%3A%3AAID-AJMG1282%3E3.0.CO%3B2-7

Genetically defined therapy of inherited long-QT syndrome. Correction of abnormal repolarization by potassium

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200024%2997%3A4%3C310%3A%3AAID-AJMG1282%3E3.0.CO%3B2-7

Skeletal muscle expression and abnormal function of beta-myosin in hypertrophic cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200024%2997%3A4%3C310%3A%3AAID-AJMG1282%3E3.0.CO%3B2-7

Mapping of a first locus for autosomal dominant myxomatous mitral-valve prolapse to chromosome 16p11.2-p12.1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200024%2997%3A4%3C310%3A%3AAID-AJMG1282%3E3.0.CO%3B2-7

Ionic mechanisms responsible for the electrocardiographic phenotype of the Brugada syndrome are temperature dependent

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200024%2997%3A4%3C310%3A%3AAID-AJMG1282%3E3.0.CO%3B2-7

Prognostic determinants in hypertrophic cardiomyopathy. Prospective evaluation of a therapeutic strategy based on clinical, Holter, hemodynamic, and electrophysiological findings

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200024%2997%3A4%3C310%3A%3AAID-AJMG1282%3E3.0.CO%3B2-7

A molecular basis for familial hypertrophic cardiomyopathy: a beta cardiac myosin heavy chain gene missense mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200024%2997%3A4%3C310%3A%3AAID-AJMG1282%3E3.0.CO%3B2-7

Congenital deaf-mutism, functional heart disease with prolongation of the Q-T interval and sudden death

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200024%2997%3A4%3C310%3A%3AAID-AJMG1282%3E3.0.CO%3B2-7

Mutations in the cardiac troponin I gene associated with hypertrophic cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200024%2997%3A4%3C310%3A%3AAID-AJMG1282%3E3.0.CO%3B2-7

The locus of a novel gene responsible for arrhythmogenic right-ventricular dysplasia characterized by early onset and high penetrance maps to chromosome 10p12-p14.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200024%2997%3A4%3C310%3A%3AAID-AJMG1282%3E3.0.CO%3B2-7

Desmin mutation responsible for idiopathic dilated cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200024%2997%3A4%3C310%3A%3AAID-AJMG1282%3E3.0.CO%3B2-7

Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200024%2997%3A4%3C310%3A%3AAID-AJMG1282%3E3.0.CO%3B2-7

Familial Hypertrophic cardiomyopathy with Wolff-Parkinson-White syndrome maps to a locus on chromosome 7q3

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200024%2997%3A4%3C310%3A%3AAID-AJMG1282%3E3.0.CO%3B2-7

Recent advances in the molecular genetics of hypertrophic cardiomyopathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200024%2997%3A4%3C310%3A%3AAID-AJMG1282%3E3.0.CO%3B2-7

Molecular genetic basis of hypertrophic cardiomyopathy: genetic markers for sudden cardiac death

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200024%2997%3A4%3C310%3A%3AAID-AJMG1282%3E3.0.CO%3B2-7

Angiotensin-converting enzyme polymorphism in hypertrophic cardiomyopathy and sudden cardiac death

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200024%2997%3A4%3C310%3A%3AAID-AJMG1282%3E3.0.CO%3B2-7

Identification of a deletion in plakoglobin in arrhythmogenic right ventricular cardiomyopathy with palmoplantar keratoderma and woolly hair (Naxos disease).

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200024%2997%3A4%3C310%3A%3AAID-AJMG1282%3E3.0.CO%3B2-7

Arrhythmogenic marker for the sudden unexplained death syndrome in Thai men.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200024%2997%3A4%3C310%3A%3AAID-AJMG1282%3E3.0.CO%3B2-7

A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200024%2997%3A4%3C310%3A%3AAID-AJMG1282%3E3.0.CO%3B2-7

A novel genetic pathway for sudden cardiac death via defects in the transition between ventricular and conduction system cell lineages

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200024%2997%3A4%3C310%3A%3AAID-AJMG1282%3E3.0.CO%3B2-7

Mapping a cardiomyopathy locus to chromosome 3p22-p25.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200024%2997%3A4%3C310%3A%3AAID-AJMG1282%3E3.0.CO%3B2-7

Actin mutations in dilated cardiomyopathy, a heritable form of heart failure

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200024%2997%3A4%3C310%3A%3AAID-AJMG1282%3E3.0.CO%3B2-7

Functional defects of a muscle-specific calpain, p94, caused by mutations associated with limb-girdle muscular dystrophy type 2A

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200024%2997%3A4%3C310%3A%3AAID-AJMG1282%3E3.0.CO%3B2-7

Mutations in either the essential or regulatory light chains of myosin are associated with a rare myopathy in human heart and skeletal muscle

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200024%2997%3A4%3C310%3A%3AAID-AJMG1282%3E3.0.CO%3B2-7

The gene for arrhythmogenic right ventricular cardiomyopathy maps to chromosome 14q23-q24

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200024%2997%3A4%3C310%3A%3AAID-AJMG1282%3E3.0.CO%3B2-7

A new locus for arrhythmogenic right ventricular cardiomyopathy (ARVD2) maps to chromosome 1q42-q43

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200024%2997%3A4%3C310%3A%3AAID-AJMG1282%3E3.0.CO%3B2-7

Three-dimensional structure of myosin subfragment-1: a molecular motor

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200024%2997%3A4%3C310%3A%3AAID-AJMG1282%3E3.0.CO%3B2-7

Multiple mechanisms in the long-QT syndrome. Current knowledge, gaps, and future directions. The SADS Foundation Task Force on LQTS.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200024%2997%3A4%3C310%3A%3AAID-AJMG1282%3E3.0.CO%3B2-7

Long QT syndrome patients with mutations of the SCN5A and HERG genes have differential responses to Na+ channel blockade and to increases in heart rate. Implications for gene-specific therapy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200024%2997%3A4%3C310%3A%3AAID-AJMG1282%3E3.0.CO%3B2-7

A new locus for arrhythmogenic right ventricular dysplasia on the long arm of chromosome 14.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200024%2997%3A4%3C310%3A%3AAID-AJMG1282%3E3.0.CO%3B2-7

Alpha-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomere

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200024%2997%3A4%3C310%3A%3AAID-AJMG1282%3E3.0.CO%3B2-7

Sudden unexplained death syndrome in north-east Thailand

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200024%2997%3A4%3C310%3A%3AAID-AJMG1282%3E3.0.CO%3B2-7

Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200024%2997%3A4%3C310%3A%3AAID-AJMG1282%3E3.0.CO%3B2-7

SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200024%2997%3A4%3C310%3A%3AAID-AJMG1282%3E3.0.CO%3B2-7

Congenital familial nodal rhythm

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200024%2997%3A4%3C310%3A%3AAID-AJMG1282%3E3.0.CO%3B2-7

Familial Wolff-Parkinson-White syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200024%2997%3A4%3C310%3A%3AAID-AJMG1282%3E3.0.CO%3B2-7

Dominant inheritance of McArdle syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200024%2997%3A4%3C310%3A%3AAID-AJMG1282%3E3.0.CO%3B2-7

Familial bundle branch block

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200024%2997%3A4%3C310%3A%3AAID-AJMG1282%3E3.0.CO%3B2-7

Arrhythmogenic right ventricular dysplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200024%2997%3A4%3C310%3A%3AAID-AJMG1282%3E3.0.CO%3B2-7

Kugelberg-Welander Syndrome (Hereditary Proximal Spinal Muscular Atrophy)

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200024%2997%3A4%3C310%3A%3AAID-AJMG1282%3E3.0.CO%3B2-7

A proposed autosomal dominant method of inheritance of the Wolff-Parkinson-White syndrome and supraventricular tachycardia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200024%2997%3A4%3C310%3A%3AAID-AJMG1282%3E3.0.CO%3B2-7

Apoptosis: basic mechanisms and implications for cardiovascular disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200024%2997%3A4%3C310%3A%3AAID-AJMG1282%3E3.0.CO%3B2-7

Linkage of a cardiac arrhythmia, the long QT syndrome, and the Harvey ras-1 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200024%2997%3A4%3C310%3A%3AAID-AJMG1282%3E3.0.CO%3B2-7

Point mutations and polymorphisms in the human dystrophin gene identified in genomic DNA sequences amplified by multiplex PCR

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200024%2997%3A4%3C310%3A%3AAID-AJMG1282%3E3.0.CO%3B2-7

Pathogenesis of diverse clinical and pathological phenotypes in hypertrophic cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200024%2997%3A4%3C310%3A%3AAID-AJMG1282%3E3.0.CO%3B2-7

Brugada syndrome and sudden cardiac death in children

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200024%2997%3A4%3C310%3A%3AAID-AJMG1282%3E3.0.CO%3B2-7

ARVD4, a new locus for arrhythmogenic right ventricular cardiomyopathy, maps to chromosome 2 long arm

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200024%2997%3A4%3C310%3A%3AAID-AJMG1282%3E3.0.CO%3B2-7

Autosomal dominant inherited ventricular tachycardia

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200024%2997%3A4%3C310%3A%3AAID-AJMG1282%3E3.0.CO%3B2-7

Familial total atrial standstill

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%28200024%2997%3A4%3C310%3A%3AAID-AJMG1282%3E3.0.CO%3B2-7

10.1002/1096-8628(200024)97:4<310::AID-AJMG1282>3.0.CO;2-7

21 January 2018

Identifiers

DOI

1 reference

1 August 2017

1 reference

PubMed ID

11376443