Skip to Main Content

Paper Details

De novo and inherited private variants in MAP1B in periventricular nodular heterotopia.
PLoS Genet
38
2018
MAP1B, MAP1B variant, PVNH, Periventricular nodular heterotopia, epilepsy, genetic risk loci, intolerant genes, malformation of cortical development, perisylvian polymicrogyria, periventricular nodular heterotopia, sporadic diseases
Author NameAffiliation
Erin L HeinzenInstitute for Genomic Medicine, Columbia University Medical Center
Andrew S AllenCenter for Statistical Genetics and Genomics, Duke University Medical Center
Andrew S AllenDuke University
Melanie BahloThe Walter and Eliza Hall Institute of Medical Research
Melanie BahloUniversity of Melbourne
Ming-Hui ChenBoston Children's Hospital
William B DobynsUniversity of Washington
William B DobynsCenter for Integrative Brain Research, Seattle Children's Research Institute
Christopher A WalshManton Center for Orphan Disease Research and Howard Hughes Medical Institute, Boston Children's Hospital
Christopher A WalshHarvard Medical School
Christopher A WalshBroad Institute of MIT and Harvard
Christopher A WalshManton Center for Orphan Disease Research and Howard Hughes Medical Institute, Boston Children's Hospital
Christopher A WalshHarvard Medical School
Christopher A WalshBroad Institute of MIT and Harvard
  • 1 - 14

Datasets

Release 1.2