Additional file 4 of Coding and noncoding variants in EBF3 are involved in HADDS and simplex autism

Additional file 4: Table S8: Protein-coding de novo mutations in EBF3 from Coe et al. 2019, Nature Genetics and Kaplanis et al. 2020, bioRxiv.补充文件4：表S8：EBF3基因的编码蛋白新发突变，数据源自Coe等人2019年发表于《自然·遗传学》（Nature Genetics）的研究，以及Kaplanis等人2020年发布于bioRxiv的成果。