Rare inherited missense variants of POGZ associate with autism risk and disrupt neuronal development-Reference-Cited by-同舟云学术

Rare inherited missense variants of POGZ associate with autism risk and disrupt neuronal development

Published:2019-05 Issue:5 Volume:46 Page:247-257
ISSN:1673-8527
Container-title:Journal of Genetics and Genomics
language:en
Short-container-title:Journal of Genetics and Genomics

Author:

Zhao Wenjing,Tan Jieqiong,Zhu Tengfei,Ou Jianjun,Li Ying,Shen Lu,Wu Huidan,Han Lin,Liu Yanling,Jia Xiangbin,Bai Ting,Li Honghui,Ke Xiaoyan,Zhao Jingping,Zou Xiaobing,Hu Zhengmao,Guo Hui,Xia Kun

Funder

National Natural Science Foundation of China

Natural Science Foundation of Hunan Province

Central South University

Publisher

Elsevier BV

Subject

Genetics,Molecular Biology

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3. The emerging picture of autism spectrum disorder: genetics and pathology;Chen;Annu. Rev. Pathol.,2015

4. Regulatory activities of transposable elements: from conflicts to benefits;Chuong;Nat. Rev. Genet.,2017

5. Lens epithelium-derived growth factor (LEDGF/p75) expression in fetal and adult human brain;Chylack;Exp. Eye Res.,2004

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