Associated Papers
OCLN gene variants identified in three patients with severe neurodevelopmental disorder associated with epilepsy, intellectual disability and malformation of cortical development.
Oner TO et al.
Epileptic Disorders : International Epilepsy Journal With Videotape, 2021
Band-like calcification with simplified gyration and polymicrogyria: report of 10 new families and identification of five novel OCLN mutations.
Abdel-Hamid MS et al.
Journal of Human Genetics, 2017
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