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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Dettagli Bibliografici
Pubblicato in:Mol Genet Genomic Med
Autori principali: Han, Lin, Chen, Meilin, Wang, Yazhe, Wu, Huidan, Quan, Yingting, Bai, Ting, Li, Kuokuo, Duan, Guiqin, Gao, Yan, Hu, Zhengmao, Xia, Kun, Guo, Hui
Natura: Artigo
Lingua:Inglês
Pubblicazione: John Wiley and Sons Inc. 2019
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Original Articles
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC6625093/
https://ncbi.nlm.nih.gov/pubmed/31199603
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.789
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