Mutational analysis of two positional candidate susceptibility genes for bipolar disorder on chromosome 12q23-q24: Phenylalanine hydroxylase and human LIM-homeobox LHX5

Psychiatric Genetics

Volumn 13, Issue 2, 2003, Pages 97-101

  Green, Elaine K ^a,b   Elvidge, Gareth P ^a   Owen, Michael J ^b   Craddock, Nick ^a,b  

^a UNIVERSITY OF BIRMINGHAM   (United Kingdom)

^b CARDIFF UNIVERSITY   (United Kingdom)

Author keywords

Bipolar disorder; Chromosome 12q23 24.1; Human LIM homeobox LHX5; Phenylalanine hydroxylase

Indexed keywords

LIM PROTEIN; PHENYLALANINE 4 MONOOXYGENASE;

ADULT; ARTICLE; BASE PAIRING; BIPOLAR DISORDER; CHROMOSOME 12Q; CHROMOSOME ANALYSIS; CLINICAL ARTICLE; CONTROLLED STUDY; DNA FLANKING REGION; FEMALE; GENE DELETION; GENE IDENTIFICATION; GENE LOCATION; GENE SEQUENCE; GENETIC LINKAGE; GENETIC SCREENING; GENETIC SUSCEPTIBILITY; GENETIC VARIABILITY; HOMEOBOX; HUMAN; INTRON; LIQUID CHROMATOGRAPHY; MALE; MUTATIONAL ANALYSIS; NUCLEOTIDE SEQUENCE; PEDIGREE; PRIORITY JOURNAL; SEGREGATION ANALYSIS; SINGLE NUCLEOTIDE POLYMORPHISM;

AFRICAN CONTINENTAL ANCESTRY GROUP; BASE SEQUENCE; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 12; DNA MUTATIONAL ANALYSIS; DNA PRIMERS; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HOMEODOMAIN PROTEINS; HUMANS; INTRONS; LOD SCORE; MALE; MOOD DISORDERS; NERVE TISSUE PROTEINS; PEDIGREE; PHENYLALANINE HYDROXYLASE; POLYMERASE CHAIN REACTION; VARIATION (GENETICS); ZINC FINGERS;

EID: 0038348443     PISSN: 09558829     EISSN: None     Source Type: Journal    
DOI: 10.1097/00041444-200306000-00007     Document Type: Article

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