Functional Characterization of Bestrophin-1 Missense Mutations Associated with Autosomal Recessive Bestrophinopathy-Reference-Cited by-同舟云学术

Functional Characterization of Bestrophin-1 Missense Mutations Associated with Autosomal Recessive Bestrophinopathy

Published:2011-05-31 Issue:6 Volume:52 Page:3730
ISSN:1552-5783
Container-title:Investigative Opthalmology & Visual Science
language:en
Short-container-title:Invest. Ophthalmol. Vis. Sci.

Author:

Davidson Alice E.¹,Millar Ian D.²,Burgess-Mullan Rosemary¹,Maher Geoffrey J.¹,Urquhart Jill E.³,Brown Peter D.²,Black Graeme C. M.⁴,Manson Forbes D. C.¹

Affiliation:

1. From the School of Biomedicine, The University of Manchester, Manchester Academic Health Science Centre, Central Manchester University Hospitals, NHS Foundation Trust, Manchester, United Kingdom;

2. Faculty of Life Sciences, The University of Manchester, Manchester, United Kingdom;

3. National Genetics Reference Laboratory, St. Mary's Hospital, Manchester, United Kingdom; and

4. From the School of Biomedicine, The University of Manchester, Manchester Academic Health Science Centre, Central Manchester University Hospitals, NHS Foundation Trust, Manchester, United Kingdom; 4Manchester Royal Eye Hospital, Central Manchester Universi

Publisher

Association for Research in Vision and Ophthalmology (ARVO)

Subject

General Medicine

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