Whole Exome Sequencing and Segregation Analysis Confirms That a Mutation in COL17A1 Is the Cause of Epithelial Recurrent Erosion Dystrophy in a Large Dominant Pedigree Previously Mapped to Chromosome 10q23-q24

• Benjamin R. Lin,

  Affiliation Stein Eye Institute, David Geffen School of Medicine at UCLA, Los Angeles, California, United States of America

  http://orcid.org/0000-0002-6035-2468

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• Derek J. Le,

  Affiliation Stein Eye Institute, David Geffen School of Medicine at UCLA, Los Angeles, California, United States of America

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• Yabin Chen,

  Affiliation Ophthalmic Genetics and Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, Maryland, United States of America

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• Qiwei Wang,

  Affiliation Ophthalmic Genetics and Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, Maryland, United States of America

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• D. Doug Chung,

  Affiliation Stein Eye Institute, David Geffen School of Medicine at UCLA, Los Angeles, California, United States of America

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• Ricardo F. Frausto,

  Affiliation Stein Eye Institute, David Geffen School of Medicine at UCLA, Los Angeles, California, United States of America

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• Christopher Croasdale,

  Affiliation Davis Duehr Dean Clinic, Madison, Wisconsin, United States of America

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• Richard W. Yee,

  Affiliation Cross Ophthalmology Associates, Houston, Texas, United States of America

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• Fielding J. Hejtmancik,

  Affiliation Ophthalmic Genetics and Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, Maryland, United States of America

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• Anthony J. Aldave

  * E-mail: aldave@jsei.ucla.edu

  Affiliation Stein Eye Institute, David Geffen School of Medicine at UCLA, Los Angeles, California, United States of America

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