Non syndromic autosomal dominant long QT-syndrome

Disease ID:695
Name:Non syndromic autosomal dominant long QT-syndrome
Associated with:1 target

Targets

Cav1.2
Role:  Long QT syndrome
References:  1
Mutations:  Cav1.2 is associated with 1 mutation. Click here for details

Ligands

No ligand related data available for Non syndromic autosomal dominant long QT-syndrome

References

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1. Boczek NJ, Best JM, Tester DJ, Giudicessi JR, Middha S, Evans JM, Kamp TJ, Ackerman MJ. (2013) Exome sequencing and systems biology converge to identify novel mutations in the L-type calcium channel, CACNA1C, linked to autosomal dominant long QT syndrome. Circ Cardiovasc Genet, 6 (3): 279-89. [PMID:23677916]