A Co-segregating Microduplication of Chromosome 15q11.2 Pinpoints Two Risk Genes for Autism Spectrum Disorder

High resolution genomic copy-number analysis has shown that inherited and de novo copy-number variations contribute significantly to autism pathology, and that identification of small chromosomal aberrations related to autism will expedite the discovery of risk genes involved. Here, we report a micr...

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Détails bibliographiques
Auteurs principaux: van der Zwaag, Bert, Staal, Wouter G, Hochstenbach, Ron, Poot, Martin, Spierenburg, Henk A, de Jonge, Maretha V, Verbeek, Nienke E, van ’t Slot, R., van Es, Michael A, Staal, Frank J, Freitag, Christine M, Buizer-Voskamp, Jacobine E, Nelen, Marcel R, van den Berg, Leonard H, van Amstel, Hans K Ploos, van Engeland, Herman, Burbach, J Peter H
Format: Artigo
Langue:Inglês
Publié: 2010
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Article
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC2933514/
https://ncbi.nlm.nih.gov/pubmed/20029941
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.b.31055
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