Molecular genetic analysis of long QT syndrome in Norway indicating a high prevalence of heterozygous mutation carriers-Reference-Cited by-同舟云学术

Molecular genetic analysis of long QT syndrome in Norway indicating a high prevalence of heterozygous mutation carriers

Published:2008-01 Issue:5 Volume:68 Page:362-368
ISSN:0036-5513
Container-title:Scandinavian Journal of Clinical and Laboratory Investigation
language:en
Short-container-title:Scandinavian Journal of Clinical and Laboratory Investigation

Author:

Berge K. E.,Haugaa K. H.,Früh A.,Anfinsen O.‐G.,Gjesdal K.,Siem G.,Øyen N.,Greve G.,Carlsson A.,Rognum T. O.,Hallerud M.,Kongsgård E.,Amlie J. P.,Leren T. P.

Publisher

Informa UK Limited

Subject

Clinical Biochemistry,General Medicine

Link

http://www.tandfonline.com/doi/pdf/10.1080/00365510701765643

Reference31 articles.

1. The long QT syndrome. Prospective longitudinal study of 328 families.

2. The Spectrum of Symptoms and QT Intervals in Carriers of the Gene for the Long-QT Syndrome

3. Diagnostic criteria for the long QT syndrome. An update.

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