Genetic and functional analyses identify DISC1 as a novel callosal agenesis candidate gene

American Journal of Medical Genetics, Part A

Volumn 155, Issue 8, 2011, Pages 1865-1876

  Osbun, Nathan ^a   Li, Jiang ^a   O'Driscoll, Mary C ^b   Strominger, Zoe ^a   Wakahiro, Mari ^a   Rider, Eric ^a   Bukshpun, Polina ^a   Boland, Elena ^b   Spurrell, Cailyn H ^c   Schackwitz, Wendy ^c   Pennacchio, Len A ^c   Dobyns, William B ^d   Black, Graeme C M ^b   Sherr, Elliott H ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b UNIVERSITY OF MANCHESTER   (United Kingdom)

^c DOE JOINT GENOME INSTITUTE   (United States)

^d UNIVERSITY OF WASHINGTON   (United States)

Author keywords

Agenesis of the corpus callosum; DISC1; Genetics; Schizophrenia

Indexed keywords

MESSENGER RNA;

ADOLESCENT; ADULT; ANIMAL TISSUE; ARTICLE; BRAIN DEVELOPMENT; CHILD; CHROMOSOME 1Q; CHROMOSOME DELETION; CHROMOSOME DELETION 1; CONTROLLED STUDY; CORPUS CALLOSUM; CORPUS CALLOSUM AGENESIS; DISC1 GENE; EMBRYO; EXON; FEMALE; FUNCTIONAL ASSESSMENT; GENE; GENE MAPPING; GENE MUTATION; GENE SEQUENCE; GENETIC ANALYSIS; GENETIC VARIABILITY; HUMAN; MAJOR CLINICAL STUDY; MALE; MOUSE; NONHUMAN; PRESCHOOL CHILD; PRIORITY JOURNAL; RNA SPLICING; SCHOOL CHILD;

ABNORMALITIES, MULTIPLE; ADOLESCENT; AGENESIS OF CORPUS CALLOSUM; AMINO ACID SEQUENCE; ANIMALS; CHILD; CHILD, PRESCHOOL; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 1; CORPUS CALLOSUM; FEMALE; GENOME-WIDE ASSOCIATION STUDY; HUMANS; MALE; MICE; MOLECULAR SEQUENCE DATA; MUTATION, MISSENSE; NERVE TISSUE PROTEINS; POLYMORPHISM, SINGLE NUCLEOTIDE; SEQUENCE ALIGNMENT; SEQUENCE ANALYSIS, DNA; WOLFF-PARKINSON-WHITE SYNDROME;

EID: 79960564840     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.34081     Document Type: Article

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