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Familial segregation of a VSX1 mutation adds a new dimension to its role in the causation of keratoconus

By Preeti Paliwal, Radhika Tandon, Divya Dube, Punit Kaur and Arundhati Sharma
Topics: Research Article
Publisher: Molecular Vision
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Provided by: PubMed Central

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  14. (2002). VSX1: a gene for posterior polymorphous dystrophy and keratoconus. Hum Mol Genet