Identification of Novel Gene Variants for Autism Spectrum Disorders in the Lebanese Population Using Whole-Exome Sequencing

In our previous study, in which array CGH was used on 19 Lebanese ASD subjects and their parents, we identified rare copy number variants (CNVs) in 14 subjects. The five remaining subjects did not show any CNVs related to autism spectrum disorders (ASD). In the present complementary study, we applie...

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Detalles Bibliográficos
Autores principales: Gerges, Perla, Bitar, Tania, Laumonnier, Frederic, Marouillat, Sylviane, Nemer, Georges, Andres, Christian R., Hleihel, Walid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8871811/
https://www.ncbi.nlm.nih.gov/pubmed/35205231
http://dx.doi.org/10.3390/genes13020186

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8871811/
https://www.ncbi.nlm.nih.gov/pubmed/35205231
http://dx.doi.org/10.3390/genes13020186

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