Failure to confirm genetic association of the FXYD6 gene with schizophrenia: The Japanese population and meta-analysis

American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics

Volumn 153, Issue 6, 2010, Pages 1221-1227

  Iwata, Yasuhide ^a   Yamada, Kazuo ^b   Iwayama, Yoshimi ^b   Anitha, Ayyappan ^c   Thanseem, Ismail ^a   Toyota, Tomoko ^b   Hattori, Eiji ^b   Ohnishi, Tetsuo ^b   Maekawa, Motoko ^b   Nakamura, Kazuhiko ^a   Suzuki, Katsuaki ^c   Matsuzaki, Hideo ^d   Tsuchiya, Kenji J ^c   Suda, Shiro ^c   Sugihara, Genichi ^c   Takebayashi, Kiyokazu ^a   Yamamoto, Shigeyuki ^c   Iwata, Keiko ^c   Mori, Norio ^a,c   Yoshikawa, Takeo ^b,e  

^a HAMAMATSU UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^b RIKEN BRAIN SCIENCE INSTITUTE   (Japan)

^c Molecular Research Center for Children's Mental Development   (Japan)

^d OSAKA UNIVERSITY   (Japan)

^e JAPAN SCIENCE AND TECHNOLOGY AGENCY   (Japan)

Author keywords

FXYD domain containing ion transport regulator 6; Linkage disequilibrium; Na,K ATPase; Phosphohippolin; Polymorphism

Indexed keywords

MEMBRANE PROTEIN; PROTEIN FXYD6; UNCLASSIFIED DRUG;

ADULT; ALLELE; ARTICLE; CASE CONTROL STUDY; CONTROLLED STUDY; FEMALE; GENE FREQUENCY; GENETIC ASSOCIATION; GENETIC SUSCEPTIBILITY; GENOTYPE; HAPLOTYPE; HUMAN; JAPANESE; MAJOR CLINICAL STUDY; MALE; PRIORITY JOURNAL; SCHIZOPHRENIA; SINGLE NUCLEOTIDE POLYMORPHISM;

ADULT; ALLELES; ASIAN CONTINENTAL ANCESTRY GROUP; CASE-CONTROL STUDIES; FEMALE; GENE FREQUENCY; GENETIC PREDISPOSITION TO DISEASE; HUMANS; ION CHANNELS; JAPAN; MALE; MIDDLE AGED; POLYMORPHISM, SINGLE NUCLEOTIDE; SCHIZOPHRENIA; SODIUM-POTASSIUM-EXCHANGING ATPASE;

EID: 77956120972     PISSN: 15524841     EISSN: 1552485X     Source Type: Journal    
DOI: 10.1002/ajmg.b.31095     Document Type: Article

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