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Publications by Delphine Héron
Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy
American Journal of Human Genetics
Genetics
De Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy With Contractures, Macrocephaly, and Dyskinesias
American Journal of Human Genetics
Genetics
Genetic and Neurodevelopmental Spectrum ofSYNGAP1-associated Intellectual Disability and Epilepsy
Journal of Medical Genetics
Genetics
A Missense Mutation Within the Fork-Head Domain of the Forkhead Box G1 Gene (FOXG1) Affects Its Nuclear Localization
Human Mutation
Genetics
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