MOESM4 of Dissecting the genetic basis of comorbid epilepsy phenotypes in neurodevelopmental disorders
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https://springernature.figshare.com/articles/MOESM4_of_Dissecting_the_genetic_basis_of_comorbid_epilepsy_phenotypes_in_neurodevelopmental_disorders/10053023/1
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资源简介:
Additional file 4: Table S2a. Similar to Additional file 2: Table S2, Additional file 4: Table S2a displays a summary of analyses performed per module while requiring a CADD score greater than 15 for missense variants.
提供机构:
Hajar Amini; Fereydoun Hormozdiari; Santhosh Girirajan; Sagiv Shifman
创建时间:
2019-10-26



