A novel TUBG1 mutation with neurodevelopmental disorder caused by malformations of cortical development

Neurodevelopmental disorder caused by malformations of cortical development is a rare neurological disease. Heterozygous missense variants in the TUBG1 gene lead to malformations of human cortical development, which further result in intellectual disability, developmental retardation, and epilepsy....

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Detalles Bibliográficos
Autores principales: Shen, Ru, Zhang, Zhen, Zhuang, Yu, Yang, Xiaohong, Duan, Lifen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2021
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7935588/
https://www.ncbi.nlm.nih.gov/pubmed/33728335
http://dx.doi.org/10.1155/2021/6644274

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7935588/
https://www.ncbi.nlm.nih.gov/pubmed/33728335
http://dx.doi.org/10.1155/2021/6644274

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