MOESM5 of Dissecting the genetic basis of comorbid epilepsy phenotypes in neurodevelopmental disorders
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https://springernature.figshare.com/articles/MOESM5_of_Dissecting_the_genetic_basis_of_comorbid_epilepsy_phenotypes_in_neurodevelopmental_disorders/10053032/1
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Additional file 5: Table S4. Significant GO terms, KEGG, and Reactome pathway enrichments, and OMIM disease terms per module (p-value < 0.05).
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figshare
创建时间：
2019-10-26
