Author:
Chen Lijuan,Su Dongmei,Li Sijia,Guan Lina,Shi Cuige,Li Dianjun,Hu Shanshan,Ma Xu
Funder
National Natural Science Foundation of China
China Postdoctoral Science Foundation
Natural Science Foundation of Heilongjiang Province of China
Publisher
Springer Science and Business Media LLC
Reference56 articles.
1. Arora A., Minogue P. J., Liu X., Addison P. K., Russel-Eggitt I., Webster A. R. et al. 2008 A novel connexin50 mutation associated with congenital nuclear pulverulent cataracts. J. Med. Genet. 45, 155–160.
2. Baruch A., Greenbaum D., Levy E. T., Nielsen P. A., Gilula N. B., Kumar N. M. et al. 2001 Defining a link between gap junction communication, proteolysis, and cataract formation. J. Biol. Chem. 276, 28999–29006.
3. Benedetti E. L., Dunia I., Recouvreur M., Nicolas P., Kumar N. M. and Bloemendal H. 2000 Structural organization of gap junctions as revealed by freeze-fracture and SDS fracture-labeling. Eur. J. Cell Biol. 79, 575–582.
4. Bennett T. M. and Shiels A. 2011 A recurrent missense mutation in GJA3 associated with autosomal dominant cataract linked to chromosome 13q. Mol. Vis. 17, 2255–2262.
5. Bennett T. M., Mackay D. S., Knopf H. L. and Shiels A. 2004 A novel missense mutation in the gene for gap-junction protein alpha3 (GJA3) associated with autosomal dominant “nuclear punctate” cataracts linked to chromosome 13q. Mol. Vis. 10, 376–382.
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