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Author Report for: Fombonne E

No contact information in database for Fombonne E

    Title: Rare exonic deletions implicate the synaptic organizer Gephyrin (GPHN) in risk for autism, schizophrenia and seizures
    Lionel AC, Vaags AK, Sato D, Gazzellone MJ, Mitchell EB, Chen HY, Costain G, Walker S, Egger G and Scherer SW <22 more author(s)>
    Ref: Hum Mol Genet, 22:2055, 2013 : PubMed


    Title: Truncating mutations in NRXN2 and NRXN1 in autism spectrum disorders and schizophrenia
    Gauthier J, Siddiqui TJ, Huashan P, Yokomaku D, Hamdan FF, Champagne N, Lapointe M, Spiegelman D, Noreau A and Rouleau GA <11 more author(s)>
    Ref: Hum Genet, 130:563, 2011 : PubMed


    Title: NLGN3/NLGN4 gene mutations are not responsible for autism in the Quebec population
    Gauthier J, Bonnel A, St-Onge J, Karemera L, Laurent S, Mottron L, Fombonne E, Joober R, Rouleau GA
    Ref: American Journal of Medicine Genet B Neuropsychiatr Genet, 132B:74, 2005 : PubMed


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Please cite: Lenfant 2013 Nucleic.Acids.Res. or Marchot Chatonnet 2012 Prot.Pept Lett.
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