Molecular genetic analysis of long QT syndrome in Norway indicating a high prevalence of heterozygous mutation carriers

Author: Berge K. E.   Haugaa K. H.   Fruh A.   Anfinsen O. -G.   Gjesdal K.   Siem G.   Øyen N.   Greve G.   Carlsson A.   Rognum T. O.   Hallerud M.   Kongsgård E.   Amlie J. P.   Leren T. P.  

Publisher: Informa Healthcare

ISSN: 0036-5513

Source: Scandinavian Journal of Clinical and Laboratory Investigation, Vol.68, Iss.5, 2008-01, pp. : 362-368

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