(Q84445454)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20564468%20AND%20SRC:MED&resulttype=core&format=json

6 February 2020

title

A homozygous SCN5A mutation in a severe, recessive type of cardiac conduction disease (English)

1 reference

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6 February 2020

1 reference

1

1 reference

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6 February 2020

author name string

Michele Eiselt

2

1 reference

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6 February 2020

Matthias Paul

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20564468%20AND%20SRC:MED&resulttype=core&format=json

6 February 2020

Kathrin Sauter

4

1 reference

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6 February 2020

Birgit Stallmeyer

5

1 reference

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6 February 2020

Dirk Isbrandt

6

1 reference

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6 February 2020

Eric Schulze-Bahr

7

1 reference

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6 February 2020

publication date

1 August 2010

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6 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20564468%20AND%20SRC:MED&resulttype=core&format=json

6 February 2020

volume

31

1 reference

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6 February 2020

issue

8

1 reference

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6 February 2020

page(s)

E1609-21

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6 February 2020

Identifiers

DOI

10.1002/HUMU.21302

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20564468%20AND%20SRC:MED&resulttype=core&format=json

6 February 2020

1 reference