Varaico: Literature-Extracted Genetic Variants

Gene:SCN1B
Variant:p.E82D
Back to variants list

SCN1B

NM_001037.5:p.E82D

Associated Papers

Mutation analysis of candidate genes SCN1B, KCND3 and ANK2 in patients with clinical diagnosis of long QT syndrome.

Raudenská M et al.

Physiological Research, 2008

[Mutational analysis of LQT genes in individuals with drug induced QT interval prolongation].

Novotný T et al.

Vnitrni Lekarstvi, 2006

[The role of ergometric testing in diagnosis of latent long QT syndrome].

Novotný T et al.

Vnitrni Lekarstvi, 2000

Select a paper to view details
UCSC Genome Browser·Imprint·Privacy·Terms·Feedback·Email Updates·

Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."