Stattin, E., Boström, I. M., Winbo, A., Cederquist, K., Jonasson, J., Jonsson, B., . . . Norberg, A. (2012). Founder mutations characterise the mutation panorama in 200 Swedish index cases referred for Long QT syndrome genetic testing. BioMed Central.
Chicago-stil citatStattin, Eva-Lena, et al. Founder Mutations Characterise the Mutation Panorama in 200 Swedish Index Cases Referred for Long QT Syndrome Genetic Testing. BioMed Central, 2012.
MLA-referensStattin, Eva-Lena, et al. Founder Mutations Characterise the Mutation Panorama in 200 Swedish Index Cases Referred for Long QT Syndrome Genetic Testing. BioMed Central, 2012.
Varning: dessa hänvisningar är inte alltid fullständigt riktiga.