The usual suspects: Tyrosine hydroxylase and the serotonin transporter in affective disorders

Molecular Psychiatry

Volumn 3, Issue 2, 1998, Pages 103-105

  Collier, D A ^a   Sham, P C ^a  

^a KING'S COLLEGE LONDON   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; SEROTONIN TRANSPORTER; TYROSINE 3 MONOOXYGENASE;

AFFECTIVE NEUROSIS; DNA POLYMORPHISM; GENETIC EPISTASIS; GENETIC HETEROGENEITY; GENETIC LINKAGE; GENETIC SUSCEPTIBILITY; HAPLOTYPE; HUMAN; PRIORITY JOURNAL; PSYCHOSIS; SHORT SURVEY;

EID: 0031897337     PISSN: 13594184     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.mp.4000384     Document Type: Short Survey

References (3)

1. Serretti A, Macciardi F, Cusin C, Verga M, Pedrini S, Smeraldi E. Tyrosine hydroxylase gene in linkage disequilibrium with mood disorders. Mol Psychiatry 1998; 3: 169-174.
2. Rosenthal NE, Mazzanti CM, Barnett RL, Hardin TA, Turner EH, Lam GK et al. Role of serotonin transporter promoter repeat polymorphism (5-HTTLPR) in seasonality and seasonal affective disorder. Mol Psychiatry 1998; 3: 175-177.
3. Balciuniene J, Yuan Q-P, Engstrom C, Lindblad K, Nylander PO, Sundvall M et al. Linkage analysis of candidate loci in families with recurrent major depression. Mol Psychiatry 1998; 3: 162-168.