Article
Novel alterations of CC2D1A as a candidate gene in a Turkish sample of patients with autism spectrum disorder.
The International journal of neuroscience - 1 Nov 2022
Sener Elif Funda, Onal Muge Gulcihan, Dal Fatma, Nalbantoglu Ufuk, Ozkul Yusuf, Canatan Halit, Oztop Didem Behice
Abstract excerpt
BACKGROUND: Autism spectrum disorder (ASD) is a neurodevelopmental disorder with large genetic background, but identification of pathogenic variants has proceeded slowly because hundreds of loci are involved in this complex disorder. CC2D1A gene firstly associated with the intellectual disability (ID) in a family with a large deletion. We aimed to contribute to the literature by sequencing this gene and by this...
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