(Q22010507)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10471492%20AND%20SRC:MED&resulttype=core&format=json

12 December 2019

title

Cardiac conduction defects associate with mutations in SCN5A (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10471492%20AND%20SRC:MED&resulttype=core&format=json

Sodium voltage-gated channel alpha subunit 5

12 December 2019

main subject

1 reference

AV node cell to bundle of His cell communication

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

1

J J Schott

J J

Schott

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10471492%20AND%20SRC:MED&resulttype=core&format=json

12 December 2019

3

F Kyndt

F

Kyndt

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10471492%20AND%20SRC:MED&resulttype=core&format=json

12 December 2019

4

V Probst

V

Probst

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10471492%20AND%20SRC:MED&resulttype=core&format=json

12 December 2019

Alshinawi C

2

C

Alshinawi

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10471492%20AND%20SRC:MED&resulttype=core&format=json

12 December 2019

Hoorntje TM

5

T M

Hoorntje

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10471492%20AND%20SRC:MED&resulttype=core&format=json

12 December 2019

Hulsbeek M

6

M

Hulsbeek

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10471492%20AND%20SRC:MED&resulttype=core&format=json

12 December 2019

Wilde AA

7

A A

Wilde

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10471492%20AND%20SRC:MED&resulttype=core&format=json

12 December 2019

Escande D

8

D

Escande

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10471492%20AND%20SRC:MED&resulttype=core&format=json

12 December 2019

Mannens MM

9

M M

Mannens

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10471492%20AND%20SRC:MED&resulttype=core&format=json

12 December 2019

Le Marec H

10

H

Le Marec

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10471492%20AND%20SRC:MED&resulttype=core&format=json

12 December 2019

language of work or name

English

0 references

publication date

1 September 1999

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10471492%20AND%20SRC:MED&resulttype=core&format=json

12 December 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10471492%20AND%20SRC:MED&resulttype=core&format=json

12 December 2019

volume

23

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10471492%20AND%20SRC:MED&resulttype=core&format=json

12 December 2019

issue

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10471492%20AND%20SRC:MED&resulttype=core&format=json

12 December 2019

page(s)

20-21

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10471492%20AND%20SRC:MED&resulttype=core&format=json

ETIOLOGY AND PATHOLOGY OF BILATERAL BUNDLE BRANCH BLOCK IN RELATION TO COMPLETE HEART BLOCK.

12 December 2019

cites work

1 reference

7 January 2021

The Pathogenesis of Atrioventricular Block in Coronary Disease

1 reference

7 January 2021

Gene for progressive familial heart block type I maps to chromosome 19q13.

1 reference

7 January 2021

An isolated cardiac conduction disease maps to chromosome 19q

1 reference

7 January 2021

A gene defect that causes conduction system disease and dilated cardiomyopathy maps to chromosome 1p1-1q1

1 reference

7 January 2021

Mapping a cardiomyopathy locus to chromosome 3p22-p25.

1 reference

7 January 2021

Linkage of familial dilated cardiomyopathy with conduction defect and muscular dystrophy to chromosome 6q23.

1 reference

7 January 2021

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

1 reference

7 January 2021

Congenital heart disease caused by mutations in the transcription factor NKX2-5

1 reference

7 January 2021

Genomic organization of the human SCN5A gene encoding the cardiac sodium channel

1 reference

7 January 2021

The mutational spectrum of single base-pair substitutions in mRNA splice junctions of human genes: causes and consequences

1 reference

7 January 2021

Ionic mechanisms of propagation in cardiac tissue. Roles of the sodium and L-type calcium currents during reduced excitability and decreased gap junction coupling

1 reference

7 January 2021

Slow conduction in cardiac tissue, I: effects of a reduction of excitability versus a reduction of electrical coupling on microconduction.

1 reference

7 January 2021

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

1 reference

7 January 2021

Genetic basis and molecular mechanism for idiopathic ventricular fibrillation

1 reference

7 January 2021

Identifiers

DOI

10.1038/12618

2 references

Consolidated OpenCitations Corpus – April 2017

1412444

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10471492%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

12 December 2019

1021521722

0 references

1412444

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

2 references

1412444