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A novel frameshift mutation in UPF3B identified in brothers affected with childhood onset schizophrenia and autism spectrum disorders

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A Corrigendum to this article was published on 07 September 2010

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Authors and Affiliations

  1. Child Psychiatry Branch, National Institute of Mental Health, Bethesda, MD, USA

    A M Addington, N Gogtay, R Miller, J Tossell, J Bakalar, G Germain, P Gochman, R Long & J L Rapoport

  2. Centre of Excellence in Neuromics of Université de Montréal, Centre Hospitalier de l’Université de Montréal, Montréal, QC, Canada

    J Gauthier, A Piton, A Raymond & G A Rouleau

  3. Department of Medicine, Université of Montréal, Montréal, QC, Canada

    J Gauthier, A Piton, A Raymond & G A Rouleau

  4. Centre of Excellence in Neuromics of Université de Montréal, CHU Sainte-Justine Research Center, Montréal, QC, Canada

    F F Hamdan

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  1. A M Addington
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  2. J Gauthier
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  3. A Piton
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  4. F F Hamdan
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  5. A Raymond
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  6. N Gogtay
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  7. R Miller
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  8. J Tossell
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  9. J Bakalar
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  10. G Germain
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  11. P Gochman
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  12. R Long
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  13. J L Rapoport
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  14. G A Rouleau
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Corresponding author

Correspondence to A M Addington.

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The authors declare no conflict of interest.

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Addington, A., Gauthier, J., Piton, A. et al. A novel frameshift mutation in UPF3B identified in brothers affected with childhood onset schizophrenia and autism spectrum disorders. Mol Psychiatry 16, 238–239 (2011). https://doi.org/10.1038/mp.2010.59

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