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Paper Details

Gain and loss of function variants in EZH1 disrupt neurogenesis and cause dominant and recessive neurodevelopmental disorders.
Nat Commun
5
2023
Author NameAffiliation
Dong LiCenter for Applied Genomics, The Children's Hospital of Philadelphia
Margaret HarrCenter for Applied Genomics, The Children's Hospital of Philadelphia
Hakon HakonarsonCenter for Applied Genomics, The Children's Hospital of Philadelphia
Hakon HakonarsonCenter for Applied Genomics, The Children's Hospital of Philadelphia
Shehla MohammedGuy's Hospital
Henry HouldenQueen Square Institute of Neurology, University College London
Anna C E HurstUniversity of Alabama at Birmingham
Siddharth BankaUniversity of Manchester
Siddharth BankaSt Mary's Hospital, Manchester University NHS Foundation Trust
Deborah L FrenchRaymond G. Perelman Center for Cellular and Molecular Therapeutics, The Children's Hospital of Philadelphia
Deborah L FrenchUniversity of Pennsylvania
Elizabeth A HellerUniversity of Pennsylvania
Fowzan S AlkurayaCenter for Genomic Medicine, King Faisal Specialist Hospital and Research Center
Fowzan S AlkurayaCollege of Medicine, Alfaisal University
Pankaj B AgrawalBoston Children's Hospital
Pankaj B AgrawalBoston Children's Hospital
Pankaj B AgrawalThe Manton Center for Orphan Disease Research, Boston Children's Hospital
Pankaj B AgrawalUniversity of Miami School of Medicine and Holtz Children's Hospital
Danny ReinbergHHMI/NYU Langone School of Medicine
Naiara AkizuRaymond G. Perelman Center for Cellular and Molecular Therapeutics, The Children's Hospital of Philadelphia
Naiara AkizuUniversity of Pennsylvania
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