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napolitano c, priori sg, schwartz pj, bloise r, ronchetti e, nastoli j, bottelli g, cerrone m, leonardi s.. genetic testing in the long qt syndrome: development and validation of an efficient approach to genotyping in clinical practice. 2005 dec 21;294(23):2975-80
priori sg, pandit sv, rivolta i, berenfeld o, ronchetti e, dhamoon a, napolitano c, anumonwo j, di barletta mr, gudapakkam s, bosi g, stramba-badiale m, jalife j. a novel form of short qt syndrome (sqt3) is caused by a mutation in the kcnj2 gene. circ res. 2005 apr 15;96(7):800-7.
genetic testing in the long qt syndrome: development and validation of an efficient approach to genotyping in clinical practice. napolitano c, priori sg, schwartz pj, bloise r, ronchetti e, nastoli j, bottelli g, cerrone m, leonardi s. jama. 2005 dec 21;294(23):2975-80.
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