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

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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Bibliographic Details
Main Authors: Perla Gerges, Tania Bitar, Frederic Laumonnier, Sylviane Marouillat, Georges Nemer, Christian R. Andres, Walid Hleihel
Format: Article
Language:English
Published: MDPI AG 2022-01-01
Series:Genes
Subjects:
autism spectrum disorders
whole-exome sequ encing
single nucleotide variations
insertions/deletions
genetic etiology
<i>MIS18BP1</i>
Online Access:https://www.mdpi.com/2073-4425/13/2/186

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https://www.mdpi.com/2073-4425/13/2/186

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