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A KCNH2 branch point mutation causing aberrant splicing contributes to an explanation of genotype-negative long QT syndrome
Lia Crotti*, Marzena A. Lewandowska, Peter J. Schwartz, Roberto Insolia, Matteo Pedrazzini, Erica Bussani, Federica Dagradi, Alfred L. George, Franco Pagani
*Corresponding author for this work
Research output: Contribution to journal › Article › peer-review
31
Scopus
citations