Association study of DISC1 in Korean population with autism spectrum disorders

Psychiatric Genetics

Volumn 19, Issue 3, 2009, Pages 160-

  Lim, Sun Mi ^a   Kim, Hak Jae ^b   Nam, Min ^c   Chung, Joo Ho ^b   Park, Yoon Hyung ^a  

^a Soonchunhyang University   (South Korea)

^b Kyung Hee University Hospital   (South Korea)

^c Ewha Womans University   (South Korea)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; ALLELE; AUTISM; CASE CONTROL STUDY; CONTROLLED STUDY; DISRUPTED IN SCHIZOPHRENIA 1 GENE; FEMALE; GENE; GENE SEQUENCE; GENETIC ASSOCIATION; GENETIC CODE; GENETIC SUSCEPTIBILITY; GENOTYPE; HUMAN; INTERVIEW; KOREA; LETTER; MAJOR CLINICAL STUDY; MALE; MENTAL DISEASE; POPULATION GENETICS; PRIORITY JOURNAL; PSYCHIATRIST; SINGLE NUCLEOTIDE POLYMORPHISM; GENETICS;

DISC1 PROTEIN, HUMAN; NERVE PROTEIN;

ADULT; AUTISTIC DISORDER; CASE-CONTROL STUDIES; FEMALE; HUMANS; KOREA; MALE; NERVE TISSUE PROTEINS; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 67649202210     PISSN: 09558829     EISSN: None     Source Type: Journal    
DOI: 10.1097/YPG.0b013e32832a9bd1     Document Type: Letter

References (5)

1. American Psychiatric Association (1994). Diagnostic and Statistical Manual of Mental Disorders. 4th ed. Washington, DC: American Psychiatric Press.
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3. Maussion G, Carayol J, Lepagnol-Bestel AM, Tores F, Loe-Mie Y, Milbreta U, et al. (2008). Convergent evidence identifying MAP/microtubule affinity-regulating kinase 1 (MARK1) as a susceptibility gene for autism. Hum Mol Genet 17:2541-2551.
4. Sebat J, Lakshmi B, Malhotra D, Troge J, Lese-Martin C, Walsh T, et al. (2007). Strong association of de novo copy number mutations with autism. Science 316:445-449.
5. Yoo HJ, Cho IH, Park M, Cho E, Cho SC, Kim BN, et al. (2008). Association between PTGS2 polymorphism and autism spectrum disorders in Korean trios. Neurosci Res 62:66-69.