Showing results 17 to 18 of 18
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| Title | Author(s) | Issue Date | Views | |
|---|---|---|---|---|
Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals Journal:The American Journal of Human Genetics | 2019 | 57 | ||
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 |