MOESM3 of Dissecting the genetic basis of comorbid epilepsy phenotypes in neurodevelopmental disorders
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https://springernature.figshare.com/articles/MOESM3_of_Dissecting_the_genetic_basis_of_comorbid_epilepsy_phenotypes_in_neurodevelopmental_disorders/10053014/1
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资源简介：
Additional file 3: Table S3. Proportions of synonymous mutations in neurodevelopmental cases relative to controls. Tabs correspond to modules and respective total number of synonymous de novo variants.
提供机构：
Hajar Amini; Fereydoun Hormozdiari; Santhosh Girirajan; Sagiv Shifman
创建时间：
2019-10-26
