Functional analysis of T309I and R562S mutations associated with long QT syndrome type 1

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Authors	BÉBAROVÁ Markéta ŠVECOVÁ Olga BAIAZITOVA Larisa HOŠEK Jan NOVOTNÝ Tomáš
Year of publication	2018
Type	Appeared in Conference without Proceedings
MU Faculty or unit	Faculty of Medicine
Citation
Related projects:	Klinický význam a elektrofyziologické zhodnocení mutace c.926C>T genu KCNQ1 (p.T309I) jako možné „founder mutation“ syndromu dlouhého intervalu QT