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Keywords: Sipa1l3
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Journal Articles
Melanie Rothe, Noreen Kanwal, Petra Dietmann, Franziska A. Seigfried, Annemarie Hempel, Desiree Schütz, Dominik Reim, Rebecca Engels, Alexander Linnemann, Michael J. Schmeisser, Juergen Bockmann, Michael Kühl, Tobias M. Boeckers, Susanne J. Kühl
Journal:
Development
Development (2017) 144 (2): 321–333.
Published: 15 January 2017
... family of proteins comprises four members, SIPA1 and SIPA1L1-3. Mutations of the human SIPA1L3 gene result in congenital cataracts. In Xenopus , loss of Sipa1l3 function led to a severe eye phenotype that was distinguished by smaller eyes and lenses including lens fiber cell maturation defects. We found...
Includes: Supplementary data
