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A KCNH2 branch point mutation causing aberrant splicing contributes to an explanation of genotype-negative long QT syndrome
Crotti, Lia, Lewandowska, Marzena A., Schwartz, Peter J., Insolia, Roberto, Pedrazzini, Matteo, Bussani, Erica, Dagradi, Federica, George, Alfred L., Pagani, FrancoVolume:
6
Année:
2009
Langue:
english
DOI:
10.1016/j.hrthm.2008.10.044
Fichier:
PDF, 1012 KB
english, 2009