Skip to Main Content

Paper Details

Characterization of SETD1A haploinsufficiency in humans and Drosophila defines a novel neurodevelopmental syndrome.
Mol Psychiatry
33
2021
Author NameAffiliation
Christian GilissenDonders Institute for Brain, Radboud University Medical Center
Megan T Cho
Casie A GenettiBoston Children's Hospital/Harvard Medical School
Casie A GenettiThe Manton Center for Orphan Disease Research, Boston Children's Hospital and Harvard Medical School
Alicia CaseyBoston Children's Hospital and Harvard Medical School
David A KoolenDonders Institute for Brain, Radboud University Medical Center
Pankaj B AgrawalBoston Children's Hospital/Harvard Medical School
Pankaj B AgrawalThe Manton Center for Orphan Disease Research, Boston Children's Hospital and Harvard Medical School
Pankaj B AgrawalBoston Children's Hospital and Harvard Medical School
  • 1 - 9

Datasets

Release 1.2