Skip to Main Content

Paper Details

DYRK1A-related intellectual disability: a syndrome associated with congenital anomalies of the kidney and urinary tract.
Genet Med
17
2019
CAKUT, DYRK1A, DYRK1A pathogenic variants, DYRK1A variants, DYRK1A-related intellectual disability, DYRK1AL245R RNA, DYRK1AR205*, Dyrk1a, GD, GU, Haploinsufficiency of DYRK1A, Xenopus, Xenopus laevis, congenital anomalies of the kidney and urinary tract, genital defects, human, patient, patients, wild-type human DYRK1A RNA
Author NameAffiliation
Yuxiao XuWeill Institute for Neurosciences, University of California san francisco
Yuxiao XuUniversity of California berkeley
Pengfei LiuBaylor College of Medicine
Pengfei Liu
Pengfei LiuBaylor College of Medicine
Ian D KrantzThe Children's Hospital of Philadelphia and the Department of Pediatrics, Perelman School of medicine at University of Pennsylvania
Lihadh Al-GazaliCollege of Medicine and Health Sciences, United Arab Emirates University
Ghayda M MirzaaCenter for Integrative Brain Research, Seattle Children's Research Institute
Ghayda M MirzaaUniversity of Washington
Fernando ScagliaTexas Children's Hospital
Fernando ScagliaBaylor College of Medicine
Fernando ScagliaPrince of Wales Hospital
Helen Rankin WillseyWeill Institute for Neurosciences, University of California san francisco
Helen Rankin WillseyUniversity of California berkeley
  • 1 - 14

Datasets

Release 1.2