Genome-Wide Analyses of Exonic Copy Number Variants in a Family-Based Study Point to Novel Autism Susceptibility Genes

The genetics underlying the autism spectrum disorders (ASDs) is complex and remains poorly understood. Previous work has demonstrated an important role for structural variation in a subset of cases, but has lacked the resolution necessary to move beyond detection of large regions of potential intere...

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Detalles Bibliográficos
Autores principales: Bucan, Maja, Abrahams, Brett S., Wang, Kai, Glessner, Joseph T., Herman, Edward I., Sonnenblick, Lisa I., Alvarez Retuerto, Ana I., Imielinski, Marcin, Hadley, Dexter, Bradfield, Jonathan P., Kim, Cecilia, Gidaya, Nicole B., Lindquist, Ingrid, Hutman, Ted, Sigman, Marian, Kustanovich, Vlad, Lajonchere, Clara M., Singleton, Andrew, Kim, Junhyong, Wassink, Thomas H., McMahon, William M., Owley, Thomas, Sweeney, John A., Coon, Hilary, Nurnberger, John I., Li, Mingyao, Cantor, Rita M., Minshew, Nancy J., Sutcliffe, James S., Cook, Edwin H., Dawson, Geraldine, Buxbaum, Joseph D., Grant, Struan F. A., Schellenberg, Gerard D., Geschwind, Daniel H., Hakonarson, Hakon
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2009
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2695001/
https://www.ncbi.nlm.nih.gov/pubmed/19557195
http://dx.doi.org/10.1371/journal.pgen.1000536

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2695001/
https://www.ncbi.nlm.nih.gov/pubmed/19557195
http://dx.doi.org/10.1371/journal.pgen.1000536

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