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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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| Publicado no: | Mol Genet Genomic Med |
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| Main Authors: | , , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
John Wiley and Sons Inc.
2019
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| Assuntos: | |
| Acesso em linha: | 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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