Disruption of a brain transcription factor, NPAS3, is associated with schizophrenia amid learning disability

American Journal of Medical Genetics - Neuropsychiatric Genetics

Volumn 136 B, Issue 1, 2005, Pages 26-32

  Pickard, Ben S ^a,b   Malloy, M P ^a   Porteous, D J ^a   Blackwood, D H R ^a   Muir, W J ^a  

^a UNIVERSITY OF EDINBURGH   (United Kingdom)

^b WESTERN GENERAL HOSPITAL   (United Kingdom)

Author keywords

Chromosome aberration; Fahr syndrome; Fluorescence in situ hybridization (FISH)

Indexed keywords

TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR NPAS3; UNCLASSIFIED DRUG;

ARTICLE; BASAL GANGLION; CHROMOSOME 14Q; CHROMOSOME TRANSLOCATION; COMORBIDITY; COSMID; FAHR DISEASE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DISRUPTION; GENE LOCUS; GENE MUTATION; GENE SEQUENCE; GENETIC ASSOCIATION; GENETIC LINKAGE; HUMAN; LEARNING DISORDER; NERVE DEGENERATION; PRIORITY JOURNAL; SCHIZOPHRENIA;

ABNORMALITIES, MULTIPLE; AMINO ACID SEQUENCE; BASE SEQUENCE; BRAIN; CHROMOSOME BREAKAGE; CHROMOSOME DISORDERS; CHROMOSOMES, HUMAN, PAIR 14; CHROMOSOMES, HUMAN, PAIR 9; FAMILY HEALTH; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; LEARNING DISORDERS; MOLECULAR SEQUENCE DATA; MUTATION; NERVE TISSUE PROTEINS; SCHIZOPHRENIA; TRANSCRIPTION FACTORS; TRANSLOCATION, GENETIC;

EID: 21444461075     PISSN: 15524841     EISSN: 1552485X     Source Type: Journal    
DOI: 10.1002/ajmg.b.30204     Document Type: Article

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