Investigation of 15q11-q13, 16p11.2 and 22q13 CNVs in Autism Spectrum Disorder Brazilian Individuals with and without Epilepsy

Copy number variations (CNVs) are an important cause of ASD and those located at 15q11-q13, 16p11.2 and 22q13 have been reported as the most frequent. These CNVs exhibit variable clinical expressivity and those at 15q11-q13 and 16p11.2 also show incomplete penetrance. In the present work, through mu...

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Main Authors: Moreira, Danielle P., Griesi-Oliveira, Karina, Bossolani-Martins, Ana L., Lourenço, Naila C. V., Takahashi, Vanessa N. O., da Rocha, Kátia M., Moreira, Eloisa S., Vadasz, Estevão, Meira, Joanna Goes Castro, Bertola, Debora, Halloran, Eoghan O’, Magalhães, Tiago R., Fett-Conte, Agnes C., Passos-Bueno, Maria Rita
格式: Artigo
語言:Inglês
出版: Public Library of Science 2014
主題:
Research Article
在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC4177849/
https://ncbi.nlm.nih.gov/pubmed/25255310
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0107705
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