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Publications by Davide Mei

A Case-Control Collapsing Analysis Identifies Epilepsy Genes Implicated in Trio Sequencing Studies Focused on De Novo Mutations

PLoS Genetics
EvolutionEcologyGeneticsMolecular BiologyCancer ResearchSystematicsBehavior
2017English

Clinical Spectrum of STX1B-related Epileptic Disorders

Neurology
Neurology
2019English

Clinical and Genetic Factors Predicting Dravet Syndrome in Infants With SCN1A Mutations

Neurology
Neurology
2017English

Clinical Features and Outcome of 6 New Patients Carrying De Novo KCNB1 Gene Mutations

Neurology: Genetics
NeurologyGenetics
2017English

Pitfalls in Genetic Testing: The Story of missedSCN1Amutations

Molecular genetics & genomic medicine
GeneticsMolecular Biology
2016English

Idiopathic Epilepsies With Seizures Precipitated by Fever andSCN1AAbnormalities

Epilepsia
Neurology
2007English

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