A possible role for miRNA silencing in disease phenotype variation in Swedish transthyretin V30M carriers

Por Olsson, Malin, Norgren, Nina, Obayashi, Konen, Plante-Bordeneuve, Violaine, Suhr, Ole B, Cederquist, Kristina, Jonasson, Jenni
Publicado em 2010

Genetic screening in sudden cardiac death in the young can save future lives

Por Stattin, Eva-Lena, Westin, Ida Maria, Cederquist, Kristina, Jonasson, Jenni, Jonsson, Björn-Anders, Mörner, Stellan, Norberg, Anna, Krantz, Peter, Wisten, Aase
Publicado no Int J Legal Med (2015)

Founder mutations characterise the mutation panorama in 200 Swedish index cases referred for Long QT syndrome genetic testing

Por Stattin, Eva-Lena, Boström, Ida Maria, Winbo, Annika, Cederquist, Kristina, Jonasson, Jenni, Jonsson, Björn-Anders, Diamant, Ulla-Britt, Jensen, Steen M, Rydberg, Annika, Norberg, Anna
Publicado em 2012