WFS1 gene mutation search in depressive patients: Detection of five missense polymorphisms but no association with depression or bipolar affective disorder

Journal of Affective Disorders

Volumn 58, Issue 1, 2000, Pages 11-17

  Ohtsuki, T ^a   Ishiguro, H ^a   Yoshikawa, T ^b   Arinami, T ^a  

^a UNIVERSITY OF TSUKUBA   (Japan)

^b TOKYO MEDICAL AND DENTAL UNIVERSITY   (Japan)

Author keywords

Bipolar affective disorder; Depression; WSF1 gene mutation

Indexed keywords

DNA;

ADULT; ALLELE; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CLINICAL ARTICLE; CLINICAL TRIAL; CONTROLLED CLINICAL TRIAL; CONTROLLED STUDY; DEGENERATIVE DISEASE; DEPRESSION; DISEASE ASSOCIATION; EXON; FEMALE; GENE MUTATION; GENETIC POLYMORPHISM; GENOTYPE; HETEROZYGOSITY; HUMAN; MALE; MANIC DEPRESSIVE PSYCHOSIS; MISSENSE MUTATION; ONSET AGE; PRIORITY JOURNAL; WOLFRAM SYNDROME;

ADULT; AGED; ALLELES; BIPOLAR DISORDER; DEPRESSIVE DISORDER, MAJOR; EXONS; FEMALE; HETEROZYGOTE DETECTION; HOSPITALIZATION; HUMANS; MALE; MEMBRANE PROTEINS; MIDDLE AGED; MUTATION, MISSENSE; POLYMERASE CHAIN REACTION; POLYMORPHISM, GENETIC; POLYMORPHISM, RESTRICTION FRAGMENT LENGTH; RISK FACTORS; WOLFRAM SYNDROME;

EID: 0034176621     PISSN: 01650327     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0165-0327(99)00099-3     Document Type: Article

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