Novel alterations of CC2D1A as a candidate gene in a Turkish sample of patients with autism spectrum disorder.
作者： Elif Funda Sener , Muge Gulcihan Onal , Fatma Dal , Ufuk Nalbantoglu , Yusuf Ozkul
DOI: 10.1080/00207454.2020.1860968
关键词: Neurodevelopmental disorder 、 Turkish 、 Medicine 、 Candidate gene 、 Autism spectrum disorder 、 Genetics 、 Autism
摘要: Autism spectrum disorder (ASD) is a neurodevelopmental with large genetic background, but identification of pathogenic variants has proceeded slowly because hundreds loci are involved i...
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