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Filamin C: a novel component of the KCNE2 interactome during hypoxia

Journal article

Neethling A. et al, (2016), Cardiovascular Journal Of Africa, 27, 4 - 11

AKAP9 is a genetic modifier of congenital long-QT syndrome type 1.

Journal article

de Villiers CP. et al, (2014), Circ Cardiovasc Genet, 7, 599 - 606

Long QT syndrome - a genetic cardiac channelopathy.

Journal article

Szeliga MA. et al, (2010), Kardiol Pol, 68, 575 - 583