PRODH mutations and hyperprolinemia in a subset of schizophrenic patients

Human Molecular Genetics

Volumn 11, Issue 19, 2002, Pages 2243-2249

  Jacquet, Hélène ^a   Raux, Grégory ^a   Thibaut, Florence ^a,b   Hecketsweiler, Bernadette ^c   Houy, Emmanuelle ^a,b   Demilly, Caroline ^b   Haouzir, Sadeq ^b   Allio, Gabrielle ^b   Fouldrin, Gael ^b   Drouin, Valérie ^b   Bou, Jacqueline ^a   Petit, Michel ^a,b   Campion, Dominique ^a,b   Frébourg, Thierry ^a,b  

^a INSERM   (France)

^b ROUEN UNIVERSITY HOSPITAL   (France)

^c Department of Biochemistry ^*

Author keywords

[No Author keywords available]

Indexed keywords

PROLINE DEHYDROGENASE;

AMINO ACID BLOOD LEVEL; ARTICLE; CHROMOSOME 22Q; CHROMOSOME DELETION; CONTROLLED STUDY; DIGEORGE SYNDROME; DISEASE ASSOCIATION; DISEASE SEVERITY; FEMALE; FLUORESCENCE; GENE DELETION; GENE LOCUS; GENE MUTATION; GENE REARRANGEMENT; GENETIC SCREENING; GENETIC SUSCEPTIBILITY; GENETIC VARIABILITY; GENOMICS; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; HYPERPROLINEMIA; MAJOR CLINICAL STUDY; MALE; MISSENSE MUTATION; NEUROLOGIC DISEASE; NUCLEOTIDE SEQUENCE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; QUANTITATIVE ANALYSIS; SCHIZOPHRENIA; SEGREGATION ANALYSIS;

EID: 18544366528     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/11.19.2243     Document Type: Article

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