(Q47857406)

English

Compound mutations: a common cause of severe long-QT syndrome

scientific article published on 29 March 2004

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scholarly article

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Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/15051636

Compound mutations: a common cause of severe long-QT syndrome (English)

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/15051636

Peter Westenskow

object named as

Peter Westenskow

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Katherine Timothy

3

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Katherine W Timothy

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/15051636

author name string

Igor Splawski

2

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/15051636

Mark T Keating

4

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/15051636

Michael C Sanguinetti

5

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Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/15051636

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publication date

29 March 2004

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/15051636

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/15051636

109

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/15051636

15

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/15051636

1834-1841

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/15051636

Identifiers

10.1161/01.CIR.0000125524.34234.13

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/15051636

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/15051636

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