(Q44511630)

English

A missense mutation in a highly conserved region of CASQ2 is associated with autosomal recessive catecholamine-induced polymorphic ventricular tachycardia in Bedouin families from Israel

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

A missense mutation in a highly conserved region of CASQ2 is associated with autosomal recessive catecholamine-induced polymorphic ventricular tachycardia in Bedouin families from Israel (English)

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

0 references

1 reference

based on heuristic

inferred from title

ventricular tachycardia

1 reference

based on heuristic

inferred from title

author name string

Eldar M

1

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

Pras E

2

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

Lahat H

3

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

publication date

1 January 2002

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

Cold Spring Harbor Symposia on Quantitative Biology

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

67

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

333-337

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

Sudden cardiac death and polymorphous ventricular tachycardia in patients with normal QT intervals and normal systolic cardiac function

1 reference

https://api.crossref.org/works/10.1101%2FSQB.2002.67.333

21 January 2018

A missense mutation in a highly conserved region of CASQ2 is associated with autosomal recessive catecholamine-induced polymorphic ventricular tachycardia in Bedouin families from Israel

1 reference

https://api.crossref.org/works/10.1101%2FSQB.2002.67.333

21 January 2018

Calcium transport across the sarcoplasmic reticulum: structure and function of Ca2+-ATPase and the ryanodine receptor

1 reference

https://api.crossref.org/works/10.1101%2FSQB.2002.67.333

21 January 2018

Arrhythmic disorder mapped to chromosome 1q42-q43 causes malignant polymorphic ventricular tachycardia in structurally normal hearts

1 reference

https://api.crossref.org/works/10.1101%2FSQB.2002.67.333

21 January 2018

Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2)

1 reference

https://api.crossref.org/works/10.1101%2FSQB.2002.67.333

21 January 2018

Progress in the understanding of cardiac early afterdepolarizations and torsades de pointes: time to revise current concepts

1 reference

https://api.crossref.org/works/10.1101%2FSQB.2002.67.333

21 January 2018

Identifiers

10.1101/SQB.2002.67.333

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

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