Pathogenic missense mutation pattern of forkhead box genes in neurodevelopmental disorders

BACKGROUND: Forkhead box (FOX) proteins are a family of transcription factors. Mutations of three FOX genes, including FOXP1, FOXP2, and FOXG1, have been reported in neurodevelopmental disorders (NDDs). However, due to the lack of site‐specific statistical significance, the pathogenicity of missense...

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Detalles Bibliográficos
Autores principales: Han, Lin, Chen, Meilin, Wang, Yazhe, Wu, Huidan, Quan, Yingting, Bai, Ting, Li, Kuokuo, Duan, Guiqin, Gao, Yan, Hu, Zhengmao, Xia, Kun, Guo, Hui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6625093/
https://www.ncbi.nlm.nih.gov/pubmed/31199603
http://dx.doi.org/10.1002/mgg3.789

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6625093/
https://www.ncbi.nlm.nih.gov/pubmed/31199603
http://dx.doi.org/10.1002/mgg3.789

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