Additional file 4 of Coding and noncoding variants in EBF3 are involved in HADDS and simplex autism
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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:来自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预印本的EBF3基因蛋白质编码区新发突变
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figshare
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2021-07-14



