A family based study implicates solute carrier family 1–member 3 (SLC1A3) gene in attention-deficit/hyperactivity disorder
Turic, Darko, Langley, Kate, Williams, Hywel, Norton, Nadine, Williams, Nigel M., Moskvina, Valentina, Van den Bree, Marianne B., Owen, Michael J., Thapar, Anita and O'Donovan, Michael C. (2005) A family based study implicates solute carrier family 1–member 3 (SLC1A3) gene in attention-deficit/hyperactivity disorder. Biological Psychiatry, 57, (11), 1461-1466. (doi:10.1016/j.biopsych.2005.03.025).
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The glutamatergic system, the major excitatory neurotransmitter system in the central nervous system (CNS) has been proposed as contributing a possible role in the etiology of attention deficit hyperactivity disorder (ADHD). This is based upon observations from animal, neuroimaging, neuroanatomical and neuropsychological studies. Genes related to glutamate function are therefore good functional candidates for this disorder. The SLC1A3 (Solute Carrier Family 1, member 3) gene encodes a glial glutamate transporter which maps to chromosome 5p12, a region of linkage that coincides in two published ADHD genome scans so far. SLC1A3 is thus both a functional and positional candidate gene for ADHD
|Digital Object Identifier (DOI):||doi:10.1016/j.biopsych.2005.03.025|
|Keywords:||SLC1A3, glutamate function, polymorphisms, haplotype, attention deficit hyperactivity disorder (ADHD)|
|Subjects:||R Medicine > RC Internal medicine > RC0321 Neuroscience. Biological psychiatry. Neuropsychiatry|
|Divisions:||University Structure - Pre August 2011 > School of Psychology > Division of Clinical Neuroscience
|Date Deposited:||29 Jun 2010 10:40|
|Last Modified:||31 Mar 2016 13:22|
|RDF:||RDF+N-Triples, RDF+N3, RDF+XML, Browse.|
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