Cognitive profile in childhood myotonic dystrophy type 1: Is there a global impairment? - Angeard, Nathalie; Gargiulo, Marcela; Jacquette, Aurélia; Radvanyi, Hélène; Eymard, Bruno; Héron, Delphine (Neuromuscular disorders : NMD, 2007)
Keywords: (CTG) n; Adolescent; Age of Onset; Child; Childhood-onset form; Cognition; Cognition Disorders - genetics; Cognitive impairment; Female; Genes, X-Linked - genetics; Genes, Y-Linked - genetics; Humans; Intelligence - genetics; Learning Disorders - genetics; Male; Myotonic dystrophy; Myotonic Dystrophy - genetics; Myotonic Dystrophy - physiopathology; Myotonin-Protein Kinase; Neurology; Protein-Serine-Threonine Kinases - genetics; Transmitting parent’s sex; Trinucleotide Repeat Expansion - genetics; Trinucleotide Repeats - genetics; Myotonic dystrophy; Childhood-onset form; Transmitting parent’s sex; (CTG) n; Cognitive impairment