The genetics of cognitive epigenetics

Neuropharmacology

Volumn 80, Issue , 2014, Pages 83-94

  Kleefstra, Tjitske ^a   Schenck, Annette ^a   Kramer, Jamie M ^a   Van Bokhoven, Hans ^a,b  

^a RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

^b RADBOUD UNIVERSITY   (Netherlands)

Author keywords

Chromatin; Cognitive disorder; Epigenetic; Genetic; Intellectual disability; Mutation

Indexed keywords

NERVE PROTEIN;

ANIMAL; BIOLOGICAL MODEL; BRAIN; CHROMATIN ASSEMBLY AND DISASSEMBLY; CHROMOSOME 9; CHROMOSOME DELETION; COGNITION; COGNITION DISORDERS; CONGENITAL HEART MALFORMATION; CRANIOFACIAL MALFORMATION; ENZYMOLOGY; FACE; FACIES; FOOT MALFORMATION; GENE EXPRESSION REGULATION; GENETIC EPIGENESIS; GENETICS; HAND MALFORMATION; HUMAN; HYPOTRICHOSIS; INTELLECTUAL IMPAIRMENT; METABOLISM; MICROGNATHIA; MULTIPLE MALFORMATION SYNDROME; MUTATION; NECK; NERVE CELL; PATHOPHYSIOLOGY;

ABNORMALITIES, MULTIPLE; ANIMALS; BRAIN; CHROMATIN ASSEMBLY AND DISASSEMBLY; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 9; COGNITION; COGNITION DISORDERS; CRANIOFACIAL ABNORMALITIES; EPIGENESIS, GENETIC; FACE; FACIES; FOOT DEFORMITIES, CONGENITAL; GENE EXPRESSION REGULATION; HAND DEFORMITIES, CONGENITAL; HEART DEFECTS, CONGENITAL; HUMANS; HYPOTRICHOSIS; INTELLECTUAL DISABILITY; MICROGNATHISM; MODELS, BIOLOGICAL; MUTATION; NECK; NERVE TISSUE PROTEINS; NEURONS;

EID: 84898919088     PISSN: 00283908     EISSN: 18737064     Source Type: Journal    
DOI: 10.1016/j.neuropharm.2013.12.025     Document Type: Review

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