Deep exon resequencing of DLGAP2 as a candidate gene of autism spectrum disorders

Molecular Autism

Volumn 4, Issue 1, 2013, Pages

  Chien, Wei Hsien ^a   Gau, Susan Shur Fen ^b,c   Liao, Hsiao Mei ^b   Chiu, Yen Nan ^b   Wu, Yu Yu ^d   Huang, Yu Shu ^d   Tsai, Wen Che ^b   Tsai, Ho Min ^e   Chen, Chia Hsiang ^b,d,e  

^a FU JEN CATHOLIC UNIVERSITY   (Taiwan)

^b NATIONAL TAIWAN UNIVERSITY HOSPITAL   (Taiwan)

^c NATIONAL TAIWAN UNIVERSITY   (Taiwan)

^d CHANG GUNG UNIVERSITY COLLEGE OF MEDICINE   (Taiwan)

^e TZU CHI UNIVERSITY   (Taiwan)

Author keywords

Autism spectrum disorders; Common variants; DLGAP2; Rare variants

Indexed keywords

GENOMIC DNA; LARGE DROSOPHILA HOMOLOG ASSOCIATED PROTEIN 2; PROTEIN; UNCLASSIFIED DRUG;

ADOLESCENT; ADULT; ALLELE; ARTICLE; AUTISM; CHILD; CONTROLLED CLINICAL TRIAL; CONTROLLED STUDY; EXON; FAMILY STUDY; FEMALE; GENE; GENE FREQUENCY; GENE SEQUENCE; GENETIC ASSOCIATION; GENETIC VARIABILITY; HOMOZYGOTE; HUMAN; INFORMATION SCIENCE; INTRON; MAJOR CLINICAL STUDY; MALE; MISSENSE MUTATION; PRIORITY JOURNAL; SCHOOL CHILD; SINGLE NUCLEOTIDE POLYMORPHISM; TAIWAN;

EID: 84887893557     PISSN: None     EISSN: 20402392     Source Type: Journal    
DOI: 10.1186/2040-2392-4-26     Document Type: Article

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