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A Single Nucleotide Polymorphism at DBH, Possibly Associated with Attention-Deficit/Hyperactivity Disorder, Associates with Lower Plasma Dopamine β-Hydroxylase Activity and is in Linkage Disequilibrium with Two Putative Functional Single Nucleotide Polymorphisms

✍ Scribed by Yilang Tang; Sarah G. Buxbaum; Irwin Waldman; George M. Anderson; Cyrus P. Zabetian; Michael D. Köhnke; Joseph F. Cubells


Book ID
119197129
Publisher
Elsevier Science
Year
2006
Tongue
English
Weight
128 KB
Volume
60
Category
Article
ISSN
0006-3223

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## Abstract The __DBH__ locus controls plasma dopamine β‐hydroxylase activity (pDβH). A 5′‐upstream single nucleotide polymorphism (SNP) at __DBH__ (−1021C → T) explains ∼45% of the variance in pDβH, and a non‐synonymous SNP in exon 11 (+ 1603C → T) an additional 2%. However, that regression result