Author:
Refsgaard Lena,Holst Anders G,Sadjadieh Golnaz,Haunsø Stig,Nielsen Jonas B,Olesen Morten S
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Reference8 articles.
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2. Yang Y, Yang Y, Liang B et al: Identification of a Kir3.4 mutation in congenital long QT syndrome. Am J Hum Genet 2010; 86: 872–880.
3. Tester DJ, Valdivia C, Harris-Kerr C et al: Epidemiologic, molecular, and functional evidence suggest A572D-SCN5A should not be considered an independent LQT3-susceptibility mutation. Heart Rhythm 2010; 7: 912–919.
4. Exome Variant Server, NHLBI Exome Sequencing Project (ESP), Seattle, WA (url:
http://snp.gs.washington.edu/EVS/
) (Accessed 2011 Dec 05).
5. The Human Gene Mutation Database at the Institute of Medical Genetics in Cardiff (url:
http://www.hgmd.org/
) (Accessed 2011 Dec 05).
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