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Corrigendum for Urak et al., Hum. Mol. Genet. 15 (16) 2533-2541.
Human Molecular Genetics 2006 15(21):3272; doi:10.1093/hmg/ddl397
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© The Author 2006. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org

A GABRB3 promoter haplotype associated with childhood absence epilepsy impairs transcriptional activity

Lydia Urak1,2, Martha Feucht2,3, Nahid Fathi1, Kurt Hornik5 and Karoline Fuchs1,4

1 Division of Biochemistry and Molecular Biology, Center for Brain Research, 2 Department of Pediatrics, 3 Department of Child and Adolescent Neuropsychiatry, 4 Section of Biochemical Psychiatry, University Clinic for Psychiatry, Medical University of Vienna, Spitalgasse 4, 1090 Vienna, Austria and 5 Department of Statistics and Mathematics, Vienna University of Economics and Business Administration, 1090 Vienna, Austria

Human Molecular Genetics (2006) 16, 2533–2541; doi:10.1093/hmg/ddl397

The correct affiliation for Martha Feucht is as above.


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This Article
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Right arrow Alert me when this article is cited
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Right arrow Email this article to a friend
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Right arrow Articles by Urak, L.
Right arrow Articles by Fuchs, K.
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Right arrow Articles by Fuchs, K.
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