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Congenital and Childhood Myotonic Dystrophy type 1 - the impact on central nervous system, visual and motor function
(2009-04-14)
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 ...