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Mouse genetics reveals Barttin as a genetic modifier of Joubert syndrome

Journal: Proceedings of the National Academy of Sciences of the United States of America

Published: 2019-12-26

DOI: 10.1073/pnas.1912602117

Affiliations: 14

Authors: 15

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Institutions Share
Translational and Clinical Research Institute, Newcastle University, United Kingdom (UK) 0.32
Laboratory of Molecular Bases of Hereditary Kidney Diseases, Imagine Institute, France 0.13
Faculty of Medical Sciences, Newcastle University, United Kingdom (UK) 0.09
The Newcastle Upon Tyne Hospitals NHS Foundation Trust (NUTH), United Kingdom (UK) 0.07
Boston Children's Hospital (BCH), United States of America (USA) 0.07
Division of Nephrology, BCH, United States of America (USA) 0.07
Population and Health Sciences Institute, Newcastle University, United Kingdom (UK) 0.07
Newcastle Magnetic Resonance Centre, Newcastle University, United Kingdom (UK) 0.03
Northern Genetics Service, NUTH, United Kingdom (UK) 0.03
International Centre for Life (ICFL), United Kingdom (UK) 0.03
NIH NHGRI Medical Genetics Branch, United States of America (USA) 0.02
Johns Hopkins Children’s Center, United States of America (USA) 0.02
McKusick-Nathans Institute of Genetic Medicine, JHU, United States of America (USA) 0.02
NIHR Newcastle Biomedical Research Centre, United Kingdom (UK) 0.02

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