Publications
Export 3 results:
Auteur Title Type [ Année
Filtres: Auteur is Bourgeron, Thomas [Enlever les filtres]
.
2021.
Mutations in ACTL6B Cause Neurodevelopmental Deficits and Epilepsy and Lead to Loss of Dendrites in Human Neurons. The American Journal of Human Genetics.
.
2019. Mutations in ACTL6B Cause Neurodevelopmental Deficits and Epilepsy and Lead to Loss of Dendrites in Human Neurons.. Am J Hum Genet. 104(5):815-834.
.
2019.