Now showing items 1-1 of 1
Congenital and Childhood Myotonic Dystrophy type 1 - the impact on central nervous system, visual and motor function
Background and aims: Myotonic dystrophy type 1 (DM1) is an autosomal dominant multisystemic disorder, caused by an expanded CTG repeat on chromosome 19. The disorder can present both in children and adults. The overall ...