Association study of polymorphisms in the neutral amino acid transporter genes SLC1A4, SLC1A5 and the glycine transporter genes SLC6A5, SLC6A9 with schizophrenia

BMC Psychiatry

Volumn 8, Issue , 2008, Pages

  Deng, Xiangdong ^a   Sagata, Noriaki ^a   Takeuchi, Naoko ^a   Tanaka, Masami ^a   Ninomiya, Hideaki ^b   Iwata, Nakao ^c   Ozaki, Norio ^d   Shibata, Hiroki ^a   Fukumaki, Yasuyuki ^a  

^a KYUSHU UNIVERSITY   (Japan)

^b Fukuoka Prefectural Dazaifu Hospital   (Japan)

^c FUJITA HEALTH UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^d NAGOYA UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

EXCITATORY AMINO ACID TRANSPORTER; GLYCINE TRANSPORTER 1; GLYCINE TRANSPORTER 2; PROTEIN SLC1A4; PROTEIN SLC1A5; AMINO ACID TRANSPORTER; GLYCINE TRANSPORTER; SLC1A4 PROTEIN, HUMAN; SLC1A5 PROTEIN, HUMAN; SLC6A5 PROTEIN, HUMAN; SLC6A9 PROTEIN, HUMAN;

ADULT; ALLELE; ARTICLE; BLOOD SAMPLING; CONTROLLED STUDY; EXON; FEMALE; GENE FREQUENCY; GENE LINKAGE DISEQUILIBRIUM; GENE LOCUS; GENETIC ASSOCIATION; GENETIC POLYMORPHISM; GENETIC SUSCEPTIBILITY; GENOTYPE; HAPLOTYPE; HUMAN; JAPANESE; MAJOR CLINICAL STUDY; SCHIZOPHRENIA; SINGLE NUCLEOTIDE POLYMORPHISM; CASE CONTROL STUDY; GENETICS; HARTNUP DISEASE; MALE; MIDDLE AGED;

ALLELES; AMINO ACID TRANSPORT SYSTEM ASC; CASE-CONTROL STUDIES; EXONS; FEMALE; GENOTYPE; GLYCINE PLASMA MEMBRANE TRANSPORT PROTEINS; HAPLOTYPES; HARTNUP DISEASE; HUMANS; MALE; MIDDLE AGED; POLYMORPHISM, GENETIC; SCHIZOPHRENIA;

EID: 48649105703     PISSN: None     EISSN: 1471244X     Source Type: Journal    
DOI: 10.1186/1471-244X-8-58     Document Type: Article

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