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Autor:
A L, Pond, B K, Scheve, A T, Benedict, K, Petrecca, D R, Van Wagoner, A, Shrier, J M, Nerbonne
Publikováno v:
The Journal of biological chemistry. 275(8)
One form of inherited long QT syndrome, LQT2, results from mutations in HERG1, the human ether-a-go-go-related gene, which encodes a voltage-gated K(+) channel alpha subunit. Heterologous expression of HERG1 gives rise to K(+) currents that are simil