Bi-allelic Loss of Human APC2, Encoding Adenomatous Polyposis Coli Protein 2, Leads to Lissencephaly, Subcortical Heterotopia, and Global Developmental Delay.

Journal: American Journal of Human Genetics

Published: 2019-10-03

DOI: 10.1016/j.ajhg.2019.08.013

Affiliations: 20

Authors: 24

Go to article
Institutions Share
Department of Neurosciences, UC San Diego, United States of America (USA) 0.19
Genetics Research Centre, SGUL, United Kingdom (UK) 0.10
Department of Clinical Genetics, Erasmus MC, Netherlands 0.10
McMaster Children's Hospital, HHS, Canada 0.08
Human Genetics and Genome Research Division, NRC, Egypt 0.06
UCL Department of Neuromuscular Diseases, United Kingdom (UK) 0.06
Rady Children's Institute for Genomic Medicine, Rady Children's Hospital-San Diego, United States of America (USA) 0.06
Cerrahpaşa Faculty of Medicine, Istanbul University, Turkey 0.06
Institute for Clinical Genetics, TU Dresden, Germany 0.06
Faculty of Medicine, MUMS, Iran 0.04
Department of Human Genetics, Alexandria University, Egypt 0.04
Seattle Children's Research Institute, United States of America (USA) 0.03
Child Health Institute of New Jersey, NJMS RU, United States of America (USA) 0.02
Department of Neuroscience and Cell Biology, RWJMS RU, United States of America (USA) 0.02
Department of Pediatrics, UW, United States of America (USA) 0.02
Center for Integrative Brain Research, Seattle Children's Research Institute, United States of America (USA) 0.02
Brotman Baty Institute for Precision Medicine, United States of America (USA) 0.01
Department of Neurology, UW, United States of America (USA) 0.01

Return