Confirmation of the Type 2 Myotonic Dystrophy (CCTG) Expansion Mutation in Patients with Proximal Myotonic Myopathy/Proximal Myotonic Dystrophy of Different European Origins: A Single Shared Haplotype Indicates an Ancestral Founder EffectLinda L. Bachinski, Ralf Krahe, Bjarne Udd et al.|The American Journal of Human Genetics|2003Cited by 140
New methods for molecular diagnosis and demonstration of the (CCTG)n mutation in myotonic dystrophy type 2 (DM2)Riitta Sallinen, Bjarne Udd, Anna Vihola et al.|Neuromuscular Disorders|2004Cited by 45
Elevated MBL Concentrations Are Not an Indication of Association Between the <i>MBL2</i> Gene and Type 1 Diabetes or Diabetic NephropathyMari Kaunisto, Carol Forsblom, Johan Fagerudd et al.|Diabetes|2009Cited by 38
Association of the<i>SLC22A1</i>,<i>SLC22A2</i>, and<i>SLC22A3</i>genes encoding organic cation transporters with diabetic nephropathy and hypertensionRiitta Sallinen, Mari Kaunisto, Carol Forsblom et al.|Annals of Medicine|2010Cited by 32