Myotonic dystrophy: Genetic and cognitive perspective;Dystrophie myotonique de Steinert: Approche génétique et cognitive

Neuropsychiatrie de l'Enfance et de l'Adolescence

Volumn 52, Issue 3, 2004, Pages 175-180

  Angeard Durand, N ^a   Heron D ^a   Gargiulo, M ^a   Eymard, B ^a  

^a PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

Author keywords

(CTG)n triplet; Childhood form; Cognitive impairment; D ficit cognitif; Dystrophie myotonique de Steinert; Forme infantile; Learning disabilities; Myotonic dystrophy; Triplet CTG; Troubles des apprentissages

Indexed keywords

CHROMOSOME 19P; COGNITION; COGNITIVE DEFECT; CORRELATION ANALYSIS; DEPTH PERCEPTION; EVALUATION; GENE IDENTIFICATION; GENE MUTATION; GENETIC ASSOCIATION; HUMAN; INTELLIGENCE QUOTIENT; LEARNING; MEMORY; MENTAL DEFICIENCY; MYOTONIC DYSTROPHY; PHENOTYPE; REVIEW; SEX DETERMINATION;

EID: 2642581574     PISSN: 02229617     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.neurenf.2004.02.003     Document Type: Article

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