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01-08-2008 | Letter to the Editor

Pharmacological Probing of Type 1 Autism

Auteurs: Hari Manev, Radmila Manev

Gepubliceerd in: Journal of Autism and Developmental Disorders | Uitgave 7/2008

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Excerpt

Dear Editor, …
Literatuur
go back to reference Alarcón, M., Abrahams, B. S., Stone, J. L., Duvall, J. A., Perederiy, J. V., Bomar, J. M., et al. (2008). Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene. American Journal of Human Genetics, 82, 150–159. doi:10.1016/j.ajhg.2007.09.005.PubMedCrossRef Alarcón, M., Abrahams, B. S., Stone, J. L., Duvall, J. A., Perederiy, J. V., Bomar, J. M., et al. (2008). Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene. American Journal of Human Genetics, 82, 150–159. doi:10.​1016/​j.​ajhg.​2007.​09.​005.PubMedCrossRef
go back to reference Arking, D. E., Cutler, D. J., Brune, C. W., Teslovich, T. M., West, K., Ikeda, M., et al. (2008). A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism. American Journal of Human Genetics, 82, 160–164. doi:10.1016/j.ajhg.2007.09.015.PubMedCrossRef Arking, D. E., Cutler, D. J., Brune, C. W., Teslovich, T. M., West, K., Ikeda, M., et al. (2008). A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism. American Journal of Human Genetics, 82, 160–164. doi:10.​1016/​j.​ajhg.​2007.​09.​015.PubMedCrossRef
go back to reference Bakkaloglu, B., O’Roak, B. J., Louvi, A., Gupta, A. R., Abelson, J. F., Morgan, T. M., et al. (2008). Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders. American Journal of Human Genetics, 82, 165–173. doi:10.1016/j.ajhg.2007.09.017.PubMedCrossRef Bakkaloglu, B., O’Roak, B. J., Louvi, A., Gupta, A. R., Abelson, J. F., Morgan, T. M., et al. (2008). Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders. American Journal of Human Genetics, 82, 165–173. doi:10.​1016/​j.​ajhg.​2007.​09.​017.PubMedCrossRef
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go back to reference Welch, E. M., Barton, E. R., Zhuo, J., Tomizawa, Y., Friesen, W. J., Trifillis, P., et al. (2007). PTC124 targets genetic disorders caused by nonsense mutations. Nature, 447, 87–91.PubMedCrossRef Welch, E. M., Barton, E. R., Zhuo, J., Tomizawa, Y., Friesen, W. J., Trifillis, P., et al. (2007). PTC124 targets genetic disorders caused by nonsense mutations. Nature, 447, 87–91.PubMedCrossRef
Metagegevens
Titel
Pharmacological Probing of Type 1 Autism
Auteurs
Hari Manev
Radmila Manev
Publicatiedatum
01-08-2008
Uitgeverij
Springer US
Gepubliceerd in
Journal of Autism and Developmental Disorders / Uitgave 7/2008
Print ISSN: 0162-3257
Elektronisch ISSN: 1573-3432
DOI
https://doi.org/10.1007/s10803-008-0594-2

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