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A Mouse Model of Brittle Cornea Syndrome caused by mutation in Zfp469
View ORCID ProfileChloe M. Stanton, View ORCID ProfileAmy S. Findlay, Camilla Drake, Mohammad Z. Mustafa, Philippe Gautier, Lisa McKie, View ORCID ProfileIan J. Jackson, View ORCID ProfileVeronique Vitart
doi: https://doi.org/10.1101/2021.07.08.451591
Chloe M. Stanton
1MRC Human Genetics Unit, Institute of Genetics & Cancer, The University of Edinburgh, Western General Hospital, Crewe Road, Edinburgh, EH4 2XU
Amy S. Findlay
1MRC Human Genetics Unit, Institute of Genetics & Cancer, The University of Edinburgh, Western General Hospital, Crewe Road, Edinburgh, EH4 2XU
Camilla Drake
1MRC Human Genetics Unit, Institute of Genetics & Cancer, The University of Edinburgh, Western General Hospital, Crewe Road, Edinburgh, EH4 2XU
Mohammad Z. Mustafa
1MRC Human Genetics Unit, Institute of Genetics & Cancer, The University of Edinburgh, Western General Hospital, Crewe Road, Edinburgh, EH4 2XU
Philippe Gautier
1MRC Human Genetics Unit, Institute of Genetics & Cancer, The University of Edinburgh, Western General Hospital, Crewe Road, Edinburgh, EH4 2XU
Lisa McKie
1MRC Human Genetics Unit, Institute of Genetics & Cancer, The University of Edinburgh, Western General Hospital, Crewe Road, Edinburgh, EH4 2XU
Ian J. Jackson
1MRC Human Genetics Unit, Institute of Genetics & Cancer, The University of Edinburgh, Western General Hospital, Crewe Road, Edinburgh, EH4 2XU
Veronique Vitart
1MRC Human Genetics Unit, Institute of Genetics & Cancer, The University of Edinburgh, Western General Hospital, Crewe Road, Edinburgh, EH4 2XU
Posted July 09, 2021.
A Mouse Model of Brittle Cornea Syndrome caused by mutation in Zfp469
Chloe M. Stanton, Amy S. Findlay, Camilla Drake, Mohammad Z. Mustafa, Philippe Gautier, Lisa McKie, Ian J. Jackson, Veronique Vitart
bioRxiv 2021.07.08.451591; doi: https://doi.org/10.1101/2021.07.08.451591
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