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A recurrent mutation in CRYGD is associated with autosomal dominant congenital coralliform cataract in two unrelated Chinese families

By Guoxing Yang, Chunlei Xiong, Shanlan Li, Yuanyuan Wang and Jialiang Zhao
Topics: Research Article
Publisher: Molecular Vision
OAI identifier: oai:pubmedcentral.nih.gov:3086606
Provided by: PubMed Central

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Citations

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  2. (2001). British Congenital Cataract Interest Group. Measuring and interpreting the incidence of congenital ocular anomalies: lessons from a national study of congenital cataract in the UK. Invest Ophthalmol Vis Sci
  3. (1996). Drack AV. Infantile cataracts. Surv Ophthalmol