5 years ago

Mutation in the Zebrafish cct2 Gene Leads to Abnormalities of Cell Cycle and Cell Death in the Retina: A Model of CCT2-Related Leber Congenital Amaurosis.

Naoki Nakaya, Stanislav I Tomarev, Yuriko Minegishi
The compound heterozygous mutations in the β subunit of chaperonin containing TCP-1 (CCT), encoded by CCT2, lead to the Leber congenital amaurosis (LCA). In this study, a cct2 mutant line of zebrafish was established to investigate the role of CCT2 mutations in LCA in vertebrates.

Publisher URL: http://doi.org/10.1167/iovs.17-22919

DOI: 10.1167/iovs.17-22919

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