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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...
Autores principales: | 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 |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4177849/ https://www.ncbi.nlm.nih.gov/pubmed/25255310 http://dx.doi.org/10.1371/journal.pone.0107705 |
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