Etiological heterogeneity in autism spectrum disorders: More than 100 genetic and genomic disorders and still counting

Brain Research

Volumn 1380, Issue , 2011, Pages 42-77

  Betancur, Catalina ^a,b,c  

^a INSERM   (France)

^b CNRS   (France)

^c SORBONNE UNIVERSITÉ   (France)

Author keywords

Autism; Copy number variation; Deletion; Duplication; Intellectual disability; Mutation

Indexed keywords

ADENYLOSUCCINATE LYASE; ALDEHYDE DEHYDROGENASE; B RAF KINASE; CYCLIC AMP RESPONSIVE ELEMENT BINDING PROTEIN BINDING PROTEIN; CYCLIN DEPENDENT KINASE 5; FIBROBLAST GROWTH FACTOR RECEPTOR 2; GLYCINE AMIDINOTRANSFERASE; GUANIDINOACETATE METHYLTRANSFERASE; GUANOSINE TRIPHOSPHATASE ACTIVATING PROTEIN; GUANYLATE CYCLASE; HISTONE LYSINE METHYLTRANSFERASE; INTERLEUKIN 1 RECEPTOR ACCESSORY PROTEIN; K RAS PROTEIN; METHYL CPG BINDING PROTEIN; MITOGEN ACTIVATED PROTEIN KINASE KINASE 1; MYOCYTE ENHANCER FACTOR 2; MYOTONIC DYSTROPHY PROTEIN KINASE; NEUREXIN; NEUROFIBROMIN; NEUROLIGIN; PHENYLALANINE 4 MONOOXYGENASE; PHOSPHATIDYLINOSITOL 3,4,5 TRISPHOSPHATE 3 PHOSPHATASE; PROTEIN PRECURSOR; RING FINGER PROTEIN; SOMATOMEDIN B; SULFATASE; TRYPTOPHAN HYDROXYLASE; TUBERIN; UBIQUITIN PROTEIN LIGASE E3; VOLTAGE GATED SODIUM CHANNEL;

AUTISM; BECKWITH WIEDEMANN SYNDROME; CAT CRY SYNDROME; CHROMOSOME DELETION; DIGEORGE SYNDROME; DOWN SYNDROME; EPILEPSY; GENE; GENE DELETION; GENE DISRUPTION; GENE DUPLICATION; GENE LOCUS; GENE MUTATION; GENETIC ASSOCIATION; GENETIC DISORDER; HAPPY PUPPET SYNDROME; HUMAN; INTELLECTUAL IMPAIRMENT; JACOBSEN SYNDROME; KARYOTYPE 47,XYY; KLINEFELTER SYNDROME; MCDERMID SYNDROME; MILLER DIEKER SYNDROME; MONOSOMY; PRADER WILLI SYNDROME; PRIORITY JOURNAL; REVIEW; RUBINSTEIN SYNDROME; SEX CHROMOSOME MOSAICISM; SILVER RUSSELL SYNDROME; SMITH MAGENIS SYNDROME; SOTOS SYNDROME; SYNDROME; TURNER SYNDROME; WAGR SYNDROME; WILLIAMS BEUREN SYNDROME; WOLF HIRSCHHORN SYNDROME;

CHILD; CHILD DEVELOPMENT DISORDERS, PERVASIVE; CHILD, PRESCHOOL; GENETIC DISEASES, INBORN; GENETIC PREDISPOSITION TO DISEASE; HUMANS; INFANT; MUTATION; PHENOTYPE;

EID: 79952313620     PISSN: 00068993     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.brainres.2010.11.078     Document Type: Review

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