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Publications by Gaetan Lesca
A Recurrent De Novo PACS2 Heterozygous Missense Variant Causes Neonatal-Onset Developmental Epileptic Encephalopathy, Facial Dysmorphism, and Cerebellar Dysgenesis
American Journal of Human Genetics
Genetics
Mouse and Human Strategies Identify PTPN14 as a Modifier of Angiogenesis and Hereditary Haemorrhagic Telangiectasia
Nature Communications
Astronomy
Genetics
Molecular Biology
Biochemistry
Chemistry
Physics
Correction To: The Landscape of Epilepsy-Related GATOR1 Variants
Genetics in Medicine
Medicine
Genetics
Clinical Spectrum of STX1B-related Epileptic Disorders
Neurology
Neurology
Movement Disorders in Patients With Alternating Hemiplegia
Neurology
Neurology
Genetic and Neurodevelopmental Spectrum ofSYNGAP1-associated Intellectual Disability and Epilepsy
Journal of Medical Genetics
Genetics
Variable Clinical Expression in Patients With Mosaicism forKCNQ2mutations
American Journal of Medical Genetics, Part A
Genetics
Hereditary Hemorrhagic Telangiectasia: Evidence for Regional Founder Effects of ACVRL1 Mutations in French and Italian Patients
European Journal of Human Genetics
Genetics
