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A CRISPR/Cas9-generated mutation in the zebrafish orthologue of PPP2R3B, located within the Turner syndrome critical interval, causes idiopathic scoliosis
View ORCID ProfileMarian Seda, View ORCID ProfileBerta Crespo, Michelangelo Corcelli, Daniel P. Osborn, Dagan Jenkins
doi: https://doi.org/10.1101/413526
Marian Seda
1Genetics and Genomic Medicine Programme, UCL Institute of Child Health, London WC1N 1EH
Berta Crespo
2Developmental Biology and Cancer Programme, UCL Institute of Child Health, London WC1N 1EH
Michelangelo Corcelli
1Genetics and Genomic Medicine Programme, UCL Institute of Child Health, London WC1N 1EH
Daniel P. Osborn
3Genetics Research Centre, St George’s University of London, Cranmer Terrace, London SW17 0RE
Dagan Jenkins
1Genetics and Genomic Medicine Programme, UCL Institute of Child Health, London WC1N 1EH
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Posted July 25, 2019.
A CRISPR/Cas9-generated mutation in the zebrafish orthologue of PPP2R3B, located within the Turner syndrome critical interval, causes idiopathic scoliosis
Marian Seda, Berta Crespo, Michelangelo Corcelli, Daniel P. Osborn, Dagan Jenkins
bioRxiv 413526; doi: https://doi.org/10.1101/413526
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