whole genome of an epilepsy patient
收藏NIAID Data Ecosystem2026-03-12 收录
下载链接：
https://www.ncbi.nlm.nih.gov/bioproject/PRJNA760833
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资源简介：
Coexpression analysis indicates that the heterozygous mutations of KCNC1, CAPN3, NEFH and APOB were closely related to the clinical phenotypes of the patient, and the clinical phenotypic heterogeneity of the disease was the result of the interaction of multiple genes.
创建时间：
2021-09-05
