Failure to find association between PRODH deletion and schizophrenia [2]

Schizophrenia Research

Volumn 67, Issue 1, 2004, Pages 111-113

  Ohtsuki, Tsuyuka ^a   Tanaka, Syunsuke ^a   Ishiguro, Hiroki ^a   Noguchi, Emiko ^a   Arinami, Tadao ^a   Tanabe, Ei Ichi ^b   Yara, Kazuo ^b   Okubo, Tatsunobu ^b   Takahashi, Sakae ^b   Matsuura, Masato ^b   Sakai, Tei Ichiro ^b   Muto, Mariko ^b   Kojima, Takuya ^b   Matsushima, Eisuke ^c   Toru, Michio ^c   Inada, Toshiya ^d  

^a UNIVERSITY OF TSUKUBA   (Japan)

^b NIHON UNIVERSITY   (Japan)

^c TOKYO MEDICAL AND DENTAL UNIVERSITY   (Japan)

^d NAGOYA UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

PROLINE DEHYDROGENASE;

GENE AMPLIFICATION; GENE DELETION; GENETIC ASSOCIATION; GENETIC LINKAGE; GENETIC RISK; HAPLOTYPE; HUMAN; LETTER; LINKAGE ANALYSIS; MICROSATELLITE MARKER; PRIORITY JOURNAL; SCHIZOPHRENIA; SEQUENCE ANALYSIS; SINGLE NUCLEOTIDE POLYMORPHISM;

EID: 9144237473     PISSN: 09209964     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0920-9964(03)00160-9     Document Type: Letter

References (8)

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2. Jacquet H., Raux G., Thibaut F., Hecketsweiler B., Houy E., Demilly C., Haouzir S., Allio G., Fouldrin G., Drouin V., Bou J., Petit M., Campion D., Frebourg T. PRODH mutations and hyperprolinemia in a subset of schizophrenic patients. Hum. Mol. Genet. 11:2002;2243-2249.
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