Allele-Specific siRNA Silencing for the Common Keratin 12 Founder Mutation in Meesmann Epithelial Corneal Dystrophy-Reference-Cited by-同舟云学术

Allele-Specific siRNA Silencing for the Common Keratin 12 Founder Mutation in Meesmann Epithelial Corneal Dystrophy

Published:2013-01-17 Issue:1 Volume:54 Page:494
ISSN:1552-5783
Container-title:Investigative Opthalmology & Visual Science
language:en
Short-container-title:Invest. Ophthalmol. Vis. Sci.

Author:

Allen Edwin H. A.¹,Atkinson Sarah D.¹,Liao Haihui²,Moore Jonathan E.¹,Leslie Pedrioli Deena M.²,Smith Frances J. D.²,McLean William H. Irwin²,Moore C. B. Tara³

Affiliation:

1. From the School of Biomedical Sciences, University of Ulster, Coleraine, Northern Ireland BT52 1SA, United Kingdom; and the

2. Centre for Dermatology and Genetic Medicine, Colleges of Life Sciences and Medicine, Dentistry & Nursing, University of Dundee, Dundee DD1 5EH, Scotland.

3. From the School of Biomedical Sciences, University of Ulster, Coleraine, Northern Ireland BT52 1SA, United Kingdom; and the 2Centre for Dermatology and Genetic Medicine, Colleges of Life Sciences and Medicine, Dentistry & Nursing, University of Dundee, Du

Publisher

Association for Research in Vision and Ophthalmology (ARVO)

Subject

General Medicine

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