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Items: 7

1.

Genetics of inherited primary arrhythmia disorders.

Spears DA, Gollob MH.

Appl Clin Genet. 2015 Sep 18;8:215-33. doi: 10.2147/TACG.S55762. Review.

2.

The phenotype/genotype relation and the current status of genetic screening in hypertrophic cardiomyopathy, Marfan syndrome, and the long QT syndrome.

Burn J, Camm J, Davies MJ, Peltonen L, Schwartz PJ, Watkins H.

Heart. 1997 Aug;78(2):110-6. Review. No abstract available.

3.

Pharmacological targeting of long QT mutant sodium channels.

Wang DW, Yazawa K, Makita N, George AL Jr, Bennett PB.

J Clin Invest. 1997 Apr 1;99(7):1714-20.

4.

Is long QT syndrome entering the era of molecular diagnosis?

Priori SG.

Heart. 1997 Jan;77(1):5-6. No abstract available.

5.

Characterization of human cardiac Na+ channel mutations in the congenital long QT syndrome.

Wang DW, Yazawa K, George AL Jr, Bennett PB.

Proc Natl Acad Sci U S A. 1996 Nov 12;93(23):13200-5.

6.

Gene mapping of familial autosomal dominant dilated cardiomyopathy to chromosome 10q21-23.

Bowles KR, Gajarski R, Porter P, Goytia V, Bachinski L, Roberts R, Pignatelli R, Towbin JA.

J Clin Invest. 1996 Sep 15;98(6):1355-60.

7.

Mapping of a gene for long QT syndrome to chromosome 4q25-27.

Schott JJ, Charpentier F, Peltier S, Foley P, Drouin E, Bouhour JB, Donnelly P, Vergnaud G, Bachner L, Moisan JP, et al.

Am J Hum Genet. 1995 Nov;57(5):1114-22.

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