Citations for
1CPC, CRYGS
A novel missense mutation of CRYGS underlies congenital cataract in a Chinese family.
Zhang T, Yan L, Leng Y, Chen C, Ma L, Wang Q, Zhang J, Cao L.
Gene 675:9-14. doi: 10.1016/j.gene.2018.06.100. Epub 2018 Jun 28. 2018
2CPC, CRYGS
The cataract-causing mutation G75V promotes γS-crystallin aggregation by modifying and destabilizing the native structure.
Zhu S, Xi XB, Duan TL, Zhai Y, Li J, Yan YB, Yao K.
Int J Biol Macromol 117:807-814. doi: 10.1016/j.ijbiomac.2018.05.220. Epub 2018 May 30. 2018
3CPC, CRYGS
A G57W Mutation of CRYGS Associated with Autosomal Dominant Pulverulent Cataracts in a Chinese Family.
Yang Z, Li Q, Zhu S, Ma X.
Ophthalmic Genet 36(3):281-3. doi: 10.3109/13816810.2013.865761. No abstract available. 2015
4CPC, CRYGS
Structural analysis of the mutant protein D26G of human γS-crystallin, associated with Coppock cataract.
Karri S, Kasetti RB, Vendra VP, Chandani S, Balasubramanian D.
Mol Vis 19:1231-7. Print 2013. 2013
5CPC, CRYGS
Novel mutation in the gamma-S crystallin gene causing autosomal dominant cataract.
Vanita V, Singh JR, Singh D, Varon R, Sperling K.
Mol Vis 15:476-81. Epub 2009 Mar 4. 2009
6CPC, CRYGS
Gamma-S crystallin gene (CRYGS) mutation causes dominant progressive cortical cataract in humans.
Sun H, Ma Z, Li Y, Liu B, Li Z, Ding X, Gao Y, Ma W, Tang X, Li X, Shen Y.
J Med Genet 42(9):706-10. 2005