FARP‐1 deletion is associated with lack of response to autism treatment by early start denver model in a multiplex family

BACKGROUND: Children with autism spectrum disorder (ASD) display impressive clinical heterogeneity, also involving treatment response. Genetic variants can contribute to explain this large interindividual phenotypic variability. METHODS: Array‐CGH (a‐CGH) and whole genome sequencing (WGS) were perfo...

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Detalhes bibliográficos
Publicado no:Mol Genet Genomic Med
Main Authors: Cucinotta, Francesca, Ricciardello, Arianna, Turriziani, Laura, Calabrese, Giorgia, Briguglio, Marilena, Boncoddo, Maria, Bellomo, Fabiana, Tomaiuolo, Pasquale, Martines, Silvia, Bruschetta, Marianna, La Fauci Belponer, Francesca, Di Bella, Tiziana, Colombi, Costanza, Baccarin, Marco, Picinelli, Chiara, Castronovo, Paola, Lintas, Carla, Sacco, Roberto, Biederer, Thomas, Kellam, Barbara, Scherer, Stephen W., Persico, Antonio M.
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley and Sons Inc. 2020
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Original Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7507005/
https://ncbi.nlm.nih.gov/pubmed/32588496
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.1373
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