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3′ UTR polymorphism of the serotonin transporter gene and sudden infant death syndrome: Haplotype analysis

✍ Scribed by Brion S. Maher; Mary L. Marazita; Casey Rand; Lili Zhou; Elizabeth M. Berry-Kravis; Debra E. Weese-Mayer


Publisher
John Wiley and Sons
Year
2006
Tongue
English
Weight
89 KB
Volume
140A
Category
Article
ISSN
1552-4825

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## Abstract The association between the 10‐repeat allele of the dopamine transporter gene (__DAT__) and attention deficit hyperactivity disorder (ADHD) is uncertain. This study aimed to conduct a meta‐analysis of the association between the 10‐repeat allele of a variable number tandem repeat (VNTR)