Serotonin transporter missense mutation associated with a complex neuropsychiatric phenotype

Molecular Psychiatry

Volumn 8, Issue 11, 2003, Pages 895-

  Ozaki, N ^a   Goldman, D ^b   Kaye, W H ^c   Plotnicov, K ^c   Greenberg, B D ^d,e   Lappalainen, J ^f   Rudnick, G ^g   Murphy, D L ^h  

^a FUJITA HEALTH UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^b NATIONAL INSTITUTES OF HEALTH   (United States)

^c UNIVERSITY OF PITTSBURGH   (United States)

^d BUTLER HOSPITAL   (United States)

^e BROWN UNIVERSITY   (United States)

^f YALE UNIVERSITY   (United States)

^g YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^h NATIONAL INSTITUTE OF MENTAL HEALTH   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ISOLEUCINE; SEROTONIN TRANSPORTER; VALINE;

AMINO ACID SUBSTITUTION; ARTICLE; COMORBIDITY; GENETIC ASSOCIATION; GENETIC CODE; GENETIC EPISTASIS; HERITABILITY; HUMAN; MISSENSE MUTATION; NEUROPSYCHIATRY; OBSESSIVE COMPULSIVE DISORDER; PERSONALITY DISORDER; PRIORITY JOURNAL;

AMINO ACID SEQUENCE; ANOREXIA NERVOSA; ASPERGER SYNDROME; AUTISTIC DISORDER; CARRIER PROTEINS; FEMALE; GENOTYPE; HUMANS; MALE; MEMBRANE GLYCOPROTEINS; MEMBRANE TRANSPORT PROTEINS; MOLECULAR SEQUENCE DATA; MUTATION, MISSENSE; NERVE TISSUE PROTEINS; OBSESSIVE-COMPULSIVE DISORDER; PEDIGREE; PHENOTYPE; PHOBIC DISORDERS; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; PROTEIN STRUCTURE, TERTIARY; SEROTONIN PLASMA MEMBRANE TRANSPORT PROTEINS;

EID: 0242552619     PISSN: 13594184     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.mp.4001415     Document Type: Article

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