The Human W42R γD-Crystallin Mutant Structure Provides a Link between Congenital and Age-related Cataracts*

Author:

Ji Fangling,Jung Jinwon,Koharudin Leonardus M.I.,Gronenborn Angela M.

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry

Reference53 articles.

1. Characterization of the G91del CRYBA1/3-crystallin protein: a cause of human inherited cataract;Reddy;Hum. Mol. Genet.,2004

2. Genetic analysis of adult-onset cataract in a city-based ophthalmic hospital;Vijaya;Clin. Genet.,1997

3. Congenital and infantile cataract in the United Kingdom: underlying or associated factors;Rahi;Invest. Ophthalmol. Vis. Sci.,2000

4. Sequence analysis of βA3, βB3, and βA4 crystallins completes the identification of the major proteins in young human lens;Lampi;J. Biol. Chem.,1997

5. Congenital cataracts and their molecular genetics;Hejtmancik;Semin. Cell Dev. Biol.,2008

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