(Q33153857)

English

High-efficiency multiplex capillary electrophoresis single strand conformation polymorphism (multi-CE-SSCP) mutation screening of SCN5A: a rapid genetic approach to cardiac arrhythmia.

scientific article

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16712702%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

High-efficiency multiplex capillary electrophoresis single strand conformation polymorphism (multi-CE-SSCP) mutation screening of SCN5A: a rapid genetic approach to cardiac arrhythmia (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16712702%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

heart arrhythmia

0 references

capillary electrophoresis

0 references

electrophoresis

0 references

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16712702%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

Paula Louise Hedley

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16712702%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

Jacob Tfelt-Hansen

4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16712702%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

Jorgen K. Kanters

5

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16712702%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

author name string

Hofman-Bang J

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16712702%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

Haunsøe S

6

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16712702%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

McKenna WJ

7

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16712702%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

Christiansen M

8

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16712702%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

publication date

1 June 2006

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16712702%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

Clinical Genetics

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16712702%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

69

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16712702%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

6

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16712702%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

504-511

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16712702%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

Spectrum of mutations in long-QT syndrome genes. KVLQT1, HERG, SCN5A, KCNE1, and KCNE2

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2006.00621.X

21 January 2018

A single Na(+) channel mutation causing both long-QT and Brugada syndromes

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2006.00621.X

21 January 2018

Congenital sick sinus syndrome caused by recessive mutations in the cardiac sodium channel gene (SCN5A)

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2006.00621.X

21 January 2018

A common human SCN5A polymorphism modifies expression of an arrhythmia causing mutation

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2006.00621.X

21 January 2018

Identifiers

10.1111/J.1399-0004.2006.00621.X

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16712702%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16712702%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q33153857&oldid=1537590902"