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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Foilsithe in:Mol Genet Genomic Med
Main Authors: Han, Lin, Chen, Meilin, Wang, Yazhe, Wu, Huidan, Quan, Yingting, Bai, Ting, Li, Kuokuo, Duan, Guiqin, Gao, Yan, Hu, Zhengmao, Xia, Kun, Guo, Hui
Formáid: Artigo
Teanga:Inglês
Foilsithe: John Wiley and Sons Inc. 2019
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Original Articles
Rochtain Ar Líne: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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