Seong, Eunju

Mutations in VPS13D lead to a new recessive ataxia with spasticity and mitochondrial defects

Seong, E., Insolera, R., Dulovic, M., Kamsteeg, E., Trinh, J., Brüggemann, N., Sandford, E., Li, S., Ozel, A. B., Li, J. Z., et al. (2018) · Annals of Neurology

Genetic Neurodegenerative DiseasesHereditary Neurological Disorders

Cited by 163

Cadherins and catenins in dendrite and synapse morphogenesis

Seong, E., Yuan, L., & Arikkath, J. (2015) · Cell Adhesion & Migration

Neuroscience and Neuropharmacology ResearchGenetics and Neurodevelopmental Disorders

Cited by 105