Genomic sequencing in severe epilepsy: a step closer to precision medicine
Mariagrazia Esposito(University of Pisa), Pasquale Striano(Great Ormond Street Hospital), Alice Bonuccelli(University of Pisa), Ilaria Lagorio(Istituto Giannina Gaslini), Alessandro Orsini(University of Pisa), Diego Peroni
Expert Review of Precision Medicine and Drug Development
February 25, 2020
Cited by 1
Related Papers
Mapping the human genetic architecture of COVID-19
|Nature|2021|1.1k
Recurrent Rearrangements of Chromosome 1q21.1 and Variable Pediatric Phenotypes
|New England Journal of Medicine|2008|811
Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals
|The American Journal of Human Genetics|2019|310
The Pharmacoresistant Epilepsy: An Overview on Existent and New Emerging Therapies
|Frontiers in Neurology|2021|260
AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders
|Nature Communications|2019|252