Showing results 16 to 18 of 18
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Title | Author(s) | Issue Date | |
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Two-stage genome-wide association study identifies variants in CAMSAP1L1 as susceptibility loci for epilepsy in Chinese Journal:Human Molecular Genetics | 2012 | ||
Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals Journal:The American Journal of Human Genetics | 2019 | ||
Whole genome sequencing identified novel common risk and protective variants of antiseizure medication-induced Stevens-Johnson syndrome in Han Chinese Proceeding/Conference:41st Lorne Genome Conference | 2020 |