A Deletion Involving CD38 and BST1 Results in a Fusion Transcript in a Patient With Autism and Asthma

Autism Research

Volumn 7, Issue 2, 2014, Pages 254-263

  Ceroni, Fabiola ^a   Sagar, Angela ^c   Simpson, Nuala H ^b   Gawthrope, Alex J T ^b   Newbury, Dianne F ^b   Pinto, Dalila ^d   Francis, Sunday M ^c   Tessman, Dorothy C ^c   Cook, Edwin H ^c   Monaco, Anthony P ^b,e   Maestrini, Elena ^a   Pagnamenta, Alistair T ^b   Jacob, Suma ^c,f  

^a UNIVERSITY OF BOLOGNA   (Italy)

^b UNIVERSITY OF OXFORD   (United Kingdom)

^c UNIVERSITY OF ILLINOIS AT CHICAGO   (United States)

^d MOUNT SINAI SCHOOL OF MEDICINE   (United States)

^e TUFTS UNIVERSITY SCHOOL OF MEDICINE   (United States)

^f UNIVERSITY OF MINNESOTA   (United States)

Author keywords

Autism; CD38; CNV; Fusion transcript; Oxytocin

Indexed keywords

HYDROLASE; OXYTOCIN; ADENOSINE DIPHOSPHATE RIBOSYL CYCLASE; ADP-RIBOSYL CYCLASE 2; CD38 ANTIGEN; CD38 PROTEIN, HUMAN; GLYCOSYLPHOSPHATIDYLINOSITOL ANCHORED PROTEIN; LEUKOCYTE ANTIGEN; MEMBRANE PROTEIN;

ARTICLE; ASTHMA; AUTISM; BST1 GENE; CASE REPORT; CD38 GENE; CHROMOSOME 4P; CHROMOSOME DELETION; EXON; FEMALE; FUSION GENE; GENE; GENE DELETION; GENETIC SUSCEPTIBILITY; GENETIC TRANSCRIPTION; HUMAN; INHERITANCE; MOSAICISM; PRIORITY JOURNAL; RISK FACTOR; SIBLING; SPEECH DISORDER; ADOLESCENT; BLOOD; CHILD; CHILD DEVELOPMENT DISORDERS, PERVASIVE; GENE FUSION; GENETIC PREDISPOSITION; GENETICS; LONGITUDINAL STUDY; PHENOTYPE; SIGNAL TRANSDUCTION; SINGLE NUCLEOTIDE POLYMORPHISM;

ADOLESCENT; ADP-RIBOSYL CYCLASE; ANTIGENS, CD; ANTIGENS, CD38; ASTHMA; CHILD; CHILD DEVELOPMENT DISORDERS, PERVASIVE; CHROMOSOME DELETION; FEMALE; GENE FUSION; GENETIC PREDISPOSITION TO DISEASE; GPI-LINKED PROTEINS; HUMANS; LONGITUDINAL STUDIES; MEMBRANE GLYCOPROTEINS; OXYTOCIN; PHENOTYPE; POLYMORPHISM, SINGLE NUCLEOTIDE; SIGNAL TRANSDUCTION; TRANSCRIPTION, GENETIC;

EID: 84898854633     PISSN: 19393792     EISSN: 19393806     Source Type: Journal    
DOI: 10.1002/aur.1365     Document Type: Article

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