Analysis of variations in the NAPG gene on chromosome 18p11 in bipolar disorder

Psychiatric Genetics

Volumn 16, Issue 1, 2006, Pages 3-8

  Weller, Andrew E ^a   Dahl, John P ^a,b   Lohoff, Falk W ^a   Ferraro, Thomas N ^a   Berrettini, Wade H ^a  

^a UNIVERSITY OF PENNSYLVANIA   (United States)

^b 135b Clinical Research Building ^*  (United States)

Author keywords

Bipolar disorder; Case control; Genetics; NAPG

Indexed keywords

ARTICLE; BIPOLAR I DISORDER; CASE CONTROL STUDY; CHROMOSOME 18P; CHROMOSOME ANALYSIS; CONTROLLED STUDY; GENE; GENE FREQUENCY; GENETIC RISK; GENETIC VARIABILITY; GENOTYPE; HUMAN; MAJOR CLINICAL STUDY; NAPG GENE; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; RISK FACTOR; SINGLE NUCLEOTIDE POLYMORPHISM; STATISTICAL SIGNIFICANCE; BIOLOGY; BIPOLAR DISORDER; CHROMOSOME 18; FEMALE; GENETICS; MALE;

SOLUBLE N ETHYLMALEIMIDE SENSITIVE FACTOR ATTACHMENT PROTEIN;

BIPOLAR DISORDER; CASE-CONTROL STUDIES; CHROMOSOMES, HUMAN, PAIR 18; COMPUTATIONAL BIOLOGY; FEMALE; HUMANS; MALE; POLYMORPHISM, SINGLE NUCLEOTIDE; SOLUBLE N-ETHYLMALEIMIDE-SENSITIVE FACTOR ATTACHMENT PROTEINS;

EID: 33646690773     PISSN: 09558829     EISSN: None     Source Type: Journal    
DOI: 10.1097/01.ypg.0000180678.88169.b0     Document Type: Article

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