Biallelic Mutations in ADPRHL2, Encoding ADP-Ribosylhydrolase 3, Lead to a Degenerative Pediatric Stress-Induced Epileptic Ataxia Syndrome.

Journal: American Journal of Human Genetics

Published: 2018-07-25

DOI: 10.1016/j.ajhg.2018.07.010

Affiliations: 28

Authors: 39

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Institutions FC
UCL Neurogenetics Laboratory, United Kingdom (UK) 0.13
Faculty of Medicine, Dokuz Eylül University, Turkey 0.08
Department of Clinical Genetics, VUmc, Netherlands 0.08
Cologne Center for Genomics (CCG), UoC, Germany 0.08
Rady Children's Institute for Genomic Medicine, Rady Children's Hospital-San Diego, United States of America (USA) 0.06
Gleeson Laboratory for Pediatric Brain Diseases, United States of America (USA) 0.06
IRCCS Istituto Giannina Gaslini, Italy 0.05
Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, and Maternal and Children's Sciences (DINOGMI), University of Genova, Italy 0.05
Center for Molecular Medicine Cologne (CMMC), UoC, Germany 0.05
Center for Rare Diseases Cologne (ZSEK), UoC, Germany 0.05
Next Generation Genetic Clinic, Iran 0.04
Molecular and Clinical Sciences Research Institute, SGUL, United Kingdom (UK) 0.04
Department of Pediatrics, UoC, Germany 0.03
Department of Pediatrics, UC San Diego, United States of America (USA) 0.03
Amsterdam Neuroscience, Netherlands 0.03
Faculty of Medicine, MUMS, Iran 0.03
Rady Children's Hospital-San Diego, United States of America (USA) 0.03
Department of Medicine, UC San Diego, United States of America (USA) 0.03
Institute of Human Genetics, UoC, Germany 0.01
Pharmaceutical Technology Institute, MUMS, Iran 0.01
Targeted Drug Delivery Research Center, MUMS, Iran 0.01
Department of Pediatrics, UAEU, United Arab Emirates 0.01
Tawam Hospital, United Arab Emirates 0.01
Faculty of Medicine, Kastamonu University, Turkey 0.01

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