MOESM6 of Dissecting the genetic basis of comorbid epilepsy phenotypes in neurodevelopmental disorders
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https://springernature.figshare.com/articles/MOESM6_of_Dissecting_the_genetic_basis_of_comorbid_epilepsy_phenotypes_in_neurodevelopmental_disorders/10053041/1
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Additional file 6: Contains Table S5. Selective expression profiles for union of modules based on strength of epilepsy association (Classes 1, 2, and 3 as C1, C2, and C3, respectively), including: Cell-type specific Expression Analyses (CSEA), Specific Expression Analyses (SEA) for adult brain regions and development, and Tissue-Specific Expression Analyses (TSEA).
提供机构：
Hajar Amini; Fereydoun Hormozdiari; Santhosh Girirajan; Sagiv Shifman
创建时间：
2019-10-26
