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Paper Details

Somatic SLC35A2 variants in the brain are associated with intractable neocortical epilepsy.
Ann Neurol
82
2018
-AKT, -mTOR pathway genes, AKT, FCD, FCD1a, MCD, NLFE, PI3K, SCL35A2, SLC35A2, X-linked epileptic encephalopathies, brain-derived DNA, developmental delay, epilepsies, epilepsy, focal cortical dysplasia type Ia, focal epilepsy, focal malformations of cortical development, glycosylation defects, intractable neocortical epilepsy, leukocytes, mTOR, nonlesional focal epilepsy, variant allele
Author NameAffiliation
David ZagzagNew York University Langone Medical Center
David ZagzagNew York University Langone Medical Center
Guy M McKhannColumbia University
Gerald A GrantLucile Packard Children's Hospital at Stanford
Gerald A GrantLucile Packard Children's Hospital at Stanford
Mohamad A MikatiDuke University Medical Center
Mohamad A MikatiDuke University
Hart G W LidovBoston Children's Hospital and Department of Pathology, Harvard Medical School
Andrew S AllenDuke University
Peter B CrinoUniversity of Maryland
Erin L HeinzenInstitute for Genomic Medicine, Columbia University
Erin L HeinzenColumbia University
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