1. A DM1 family with interruptions associated with atypical symptoms and late onset but not with a milder phenotype. Issue 2 (4th November 2019) Authors: Ballester‐Lopez, Alfonsina; Koehorst, Emma; Almendrote, Miriam; Martínez‐Piñeiro, Alicia; Lucente, Giuseppe; Linares‐Pardo, Ian; Núñez‐Manchón, Judit; Guanyabens, Nicolau; Cano, Antoni; Lucia, Alejandro; Overend, Gayle; Cumming, Sarah A.; Monckton, Darren G.; Casadevall, Teresa; Isern, Irina; Sán... Journal: Human mutation Issue: Volume 41:Issue 2(2020) Page Start: 420 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗