Lack of association between tryptophan hydroxylase gene and psychotic symptomatology in schizophrenia

Schizophrenia Research

Volumn 40, Issue 2, 1999, Pages 171-172

  Serretti, A ^a   Lilli, R ^a   Lorenzi, C ^a   Lattuada, E ^a   Cusin, C ^a   Smeraldi, E ^a  

^a UNIVERSITY OF MILAN   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

TRYPTOPHAN HYDROXYLASE;

ADULT; ALLELE; DELUSION; FEMALE; GENE; GENETIC POLYMORPHISM; GENOTYPE; HUMAN; LETTER; MAJOR CLINICAL STUDY; MALE; PRIORITY JOURNAL; SCHIZOPHRENIA; SYMPTOMATOLOGY;

EID: 0032741465     PISSN: 09209964     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0920-9964(99)00040-7     Document Type: Article

References (3)

1. E.G. Jonsson D. Goldman G. Spurlock J.P. Gustavsson D.A. Nielsen M. Linnoila M.J. Owen G.C. Sedvall Tryptophan hydroxylase and catechol- O -methyltransferase gene polymorphisms: relationships to monoamine metabolite concentrations in CSF of healthy volunteers Eur. Arch. Psychiatry Clin. Neurosci. 247 1997 297 302
2. D.A. Nielsen G.L. Jenkins K.M. Stefanisko K.K. Jefferson D. Goldman Sequence, splice site and population frequency distribution analyses of the polymorphic human tryptophan hydroxylase intron 7 Brain Res. Mol. Brain Res. 45 1997 145 148
3. A. Serretti F. Macciardi E. Smeraldi Dopamine receptor D2 Ser Cys311 variant associated with disorganized symptomatology of schizophrenia Schizophr. Res. 34 1998 207 210