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Characterization of two novel knock-in mouse models of syndromic retinal ciliopathy carrying hypomorphic Sdccag8 mutations.
Zool Res. 2022 May 18;43(3):442-456. doi: 10.24272/j.issn.2095-8137.2021.387.
Zool Res. 2022.
PMID: 35503560
Free PMC article.
The carboxyl-terminal region of SDCCAG8 comprises a functional module essential for cilia formation as well as organ development and homeostasis.
Tsutsumi R, Chaya T, Tsujii T, Furukawa T.
Tsutsumi R, et al.
J Biol Chem. 2022 Mar;298(3):101686. doi: 10.1016/j.jbc.2022.101686. Epub 2022 Feb 4.
J Biol Chem. 2022.
PMID: 35131266
Free PMC article.
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