Myotonic Dystrophy Type 1: the heterogeneity of a complex disease in a global research approach 

Ballester López, Alfonsina (Date of defense: 2020-12-18)

Myotonic Dystrophy Type 1 (DM1) is a complex disease with a dominant autosomic inheritance caused by a CTG expansion at the end of the DMPK gene. This expansion is very unstable and it is known that is correlated with the ...