Altered phase diagram due to a single point mutation in human D-crystallin
Author:
Publisher
Proceedings of the National Academy of Sciences
Subject
Multidisciplinary
Reference37 articles.
1. Decrease in Protein Solubility and Cataract Formation Caused by the Pro23 to Thr Mutation in Human γD-Crystallin,
2. The P23T Cataract Mutation Causes Loss of Solubility of Folded γD-Crystallin
3. INVITED EDITORIAL The Genetics of Cataract: Our Vision Becomes Clearer
4. Novel mutations in the gamma-crystallin genes cause autosomal dominant congenital cataracts
5. Progressive juvenile-onset punctate cataracts caused by mutation of the D-crystallin gene
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