Human Genome Epidemiology Literature Finder
Rare Diseases
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Query Trace: Cerulean Cataract[original query] |
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Whole Exome Sequencing Reveals a Mutation in CRYBB2 in a Large Mexican Family with Autosomal Dominant Pulverulent Cataract. Molecular syndromology 2016 May 7 (2): 87-92. Messina-Baas Olga, Gonzalez-Garay Manuel L, González-Huerta Luz M, Toral-López Jaime, Cuevas-Covarrubias Sergio |
- Page last reviewed:Feb 1, 2024
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