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Volumn 23, Issue 1, 2013, Pages 38-
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Family-based association study of tryptophan hydroxylase 2 and serotonin 1A receptor genes in attention deficit hyperactivity disorder
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Author keywords
[No Author keywords available]
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Indexed keywords
SEROTONIN 1A RECEPTOR;
TRYPTOPHAN HYDROXYLASE 2;
ADOLESCENT;
ADULT;
ATTENTION DEFICIT DISORDER;
CHILD;
DNA POLYMORPHISM;
FEMALE;
GENE FREQUENCY;
GENETIC ASSOCIATION;
GENOTYPE;
HUMAN;
LETTER;
MAJOR CLINICAL STUDY;
MALE;
MATRIX ASSISTED LASER DESORPTION IONIZATION TIME OF FLIGHT MASS SPECTROMETRY;
PRESCHOOL CHILD;
PRIORITY JOURNAL;
RECEPTOR GENE;
SCHOOL CHILD;
TAIWAN;
ADOLESCENT;
ATTENTION DEFICIT DISORDER WITH HYPERACTIVITY;
CHILD;
FAMILY;
FEMALE;
GENETIC ASSOCIATION STUDIES;
GENETIC PREDISPOSITION TO DISEASE;
HUMANS;
MALE;
RECEPTOR, SEROTONIN, 5-HT1A;
REPRODUCIBILITY OF RESULTS;
TAIWAN;
TRYPTOPHAN HYDROXYLASE;
YOUNG ADULT;
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EID: 84871785654
PISSN: 09558829
EISSN: 14735873
Source Type: Journal
DOI: 10.1097/YPG.0b013e3283586378 Document Type: Letter |
Times cited : (10)
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References (3)
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