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

BACKGROUND: Congenital heart disease (CHD) is the most common birth defect and is often accompanied by neurodevelopmental disabilities (NDD) which increase the associated mortality. Plexin families are known to play a key role in the development of heart and the occurrence of neurodevelopmental anom...

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Detalles Bibliográficos
Autores principales: Feng, Zhiyu, Chen, Xinyuan, Li, Ting, Gao, Han, Chen, Weicheng, Gao, Yuan, Yao, Qinyu, Zhuang, Quannan, Ma, Xiaojing, Sheng, Wei, Xie, Yuquan, Huang, Guoying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2022
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9732602/
https://www.ncbi.nlm.nih.gov/pubmed/36506778
http://dx.doi.org/10.21037/tp-22-556

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9732602/
https://www.ncbi.nlm.nih.gov/pubmed/36506778
http://dx.doi.org/10.21037/tp-22-556

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