An X-linked PLXNB3 mutation identified in patients with congenital heart disease with neurodevelopmental disabilities-Reference-Cited by-同舟云学术

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An X-linked PLXNB3 mutation identified in patients with congenital heart disease with neurodevelopmental disabilities

Published:2022-11 Issue:11 Volume:11 Page:1852-1863
ISSN:2224-4336
Container-title:Translational Pediatrics
language:
Short-container-title:Transl Pediatr

Author:

Feng Zhiyu,Chen Xinyuan,Li Ting,Gao Han,Chen Weicheng,Gao Yuan,Yao Qinyu,Zhuang Quannan,Ma Xiaojing,Sheng Wei,Xie Yuquan,Huang Guoying

Publisher

AME Publishing Company

Subject

Pediatrics, Perinatology and Child Health

Link

https://tp.amegroups.com/article/download/105293/pdf

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Plexin B3 guides axons to cross the midline in vivo;Frontiers in Cellular Neuroscience;2024-04-02

2. Identification of candidate biomarkers and pathways associated with multiple sclerosis using bioinformatics and next generation sequencing data analysis;2023-12-07

3. Plexin-mediated neuronal development and neuroinflammatory responses in the nervous system;HISTOL HISTOPATHOL;2023

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