No association of FOXP2 and PTPRZ1 on 7q31 with autism from the Japanese population

Neuroscience Research

Volumn 53, Issue 1, 2005, Pages 91-94

  Marui, Tetsuya ^a   Koishi, Shinko ^b   Funatogawa, Ikuko ^c   Yamamoto, Kenji ^b   Matsumoto, Hideo ^b   Hashimoto, Ohiko ^d   Nanba, Eiji ^e   Kato, Chieko ^a   Ishijima, Michiko ^a   Watanabe, Keiichiro ^a   Kasai, Kiyoto ^a   Kato, Nobumasa ^a   Sasaki, Tsukasa ^a,c  

^a UNIVERSITY OF TOKYO   (Japan)

^b TOKAI UNIVERSITY   (Japan)

^c UNIVERSITY OF TOKYO   (Japan)

^d NAGOYA UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

^e TOTTORI UNIVERSITY   (Japan)

Author keywords

Autism; Chromosome 7q; FOXP2; Genetic association; PTPRZ1

Indexed keywords

FORKHEAD BOX P2 PROTEIN; NUCLEIC ACID BINDING PROTEIN; PROTEIN TYROSINE PHOSPHATASE RECEPTOR TYPE ZETA 1; UNCLASSIFIED DRUG;

ADOLESCENT; ADULT; ALLELE; ARTICLE; AUTISM; CHILD; CHROMOSOME 7Q; CONTROLLED STUDY; FEMALE; GENE FREQUENCY; GENOTYPE; HAPLOTYPE; HUMAN; JAPAN; MAJOR CLINICAL STUDY; MALE; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; STATISTICAL SIGNIFICANCE;

ADOLESCENT; ADULT; AUTISTIC DISORDER; CHILD; CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 7; CONFIDENCE INTERVALS; FEMALE; FORKHEAD TRANSCRIPTION FACTORS; GENE FREQUENCY; GENOTYPE; HUMANS; JAPAN; LINKAGE DISEQUILIBRIUM; MALE; ODDS RATIO; POLYMORPHISM, SINGLE NUCLEOTIDE; PROTEIN-TYROSINE-PHOSPHATASE; TRANSCRIPTION FACTORS;

EID: 23044492611     PISSN: 01680102     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.neures.2005.05.003     Document Type: Article

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