Literature DB >> 16987380

Risk-stratifying Jervell and Lange-Nielsen syndrome from clinical data.

Sergio Richter, Pedro Brugada.   

Abstract

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Year:  2006        PMID： 16987380     DOI： 10.1111/j.1540-8167.2006.00613.x

Source DB:  PubMed          Journal:  J Cardiovasc Electrophysiol        ISSN： 1045-3873


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  3 in total

1.  Jervell and Lange-Nielsen syndrome: novel compound heterozygous mutations in the KCNQ1 in a Korean family.

Authors:  Jae Suk Baek; Eun Jung Bae; Sang Yun Lee; Sung Sup Park; So Yeon Kim; Kyu Nam Jung; Chung Il Noh
Journal:  J Korean Med Sci       Date:  2010-09-20       Impact factor: 2.153

2.  Prevalence of Significant Genetic Variants in Congenital Long QT Syndrome is Largely Underestimated.

Authors:  Elena V Zaklyazminskaya; Hugues Abriel
Journal:  Front Pharmacol       Date:  2012-04-27       Impact factor: 5.810

3.  Large deletion in KCNQ1 identified in a family with Jervell and Lange-Nielsen syndrome.

Authors:  Ji Yeon Sung; Eun Jung Bae; Seungman Park; So Yeon Kim; Ye Jin Hyun; Sung Sup Park; Moon-Woo Seong
Journal:  Ann Lab Med       Date:  2014-08-21       Impact factor: 3.464
  3 in total

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