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POGZ de novo missense variants in neuropsychiatric disorders.

Wenjing ZhaoYingting QuanHuidan WuLin HanTing BaiLinya MaBin LiGuanglei XunJianjun OuJingping ZhaoZhengmao HuHui GuoKun Xia
Published in: Molecular genetics & genomic medicine (2019)
Our findings will be beneficial to the functional analysis of POGZ in ASD pathogenesis, and for genetic counseling and clinical diagnosis of patients with POGZ de novo missense variants.
Keyphrases
  • copy number
  • intellectual disability
  • autism spectrum disorder
  • genome wide
  • attention deficit hyperactivity disorder
  • smoking cessation
  • gene expression
  • working memory
  • hepatitis c virus
  • antiretroviral therapy