Showing 1 - 3 results of 3 for search 'Anthony J. Aldave', query time: 0.01s Refine Results
  1. 1
    Identification of the First De Novo UBIAD1 Gene Mutation Associated with Schnyder Corneal Dystrophy

    Identification of the First De Novo UBIAD1 Gene Mutation Associated with Schnyder Corneal Dystrophy by Benjamin R. Lin, Ricardo F. Frausto, Rosalind C. Vo, Stephan Y. Chiu, Judy L. Chen, Anthony J. Aldave

    Published 2016-01-01
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  2. 2
    Investigation of the functional impact of CHED- and FECD4-associated SLC4A11 mutations in human corneal endothelial cells.

    Investigation of the functional impact of CHED- and FECD4-associated SLC4A11 mutations in human corneal endothelial cells. by Doug D Chung, Angela C Chen, Charlene H Choo, Wenlin Zhang, Dominic Williams, Christopher G Griffis, Paul Bonezzi, Kavya Jatavallabhula, Alapakkam P Sampath, Anthony J Aldave

    Published 2024-01-01
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  3. 3
    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.

    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 M... by Benjamin R Lin, Derek J Le, Yabin Chen, Qiwei Wang, D Doug Chung, Ricardo F Frausto, Christopher Croasdale, Richard W Yee, Fielding J Hejtmancik, Anthony J Aldave

    Published 2016-01-01
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