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Ophthalmic Genetics Volume 37, 2016 - Issue 1
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Case Reports

Progressive Cone Dysfunction and Geographic Atrophy of the Macula in Late Stage Autosomal Dominant Vitreoretinochoroidopathy (ADVIRC)

Connie June ChenWilmer Eye Institute, Ophthalmology, Baltimore, MD, USACorrespondence[email protected]
&
Morton F. GoldbergWilmer Eye Institute, Ophthalmology, Baltimore, MD, USA
Pages 81-85 | Received 05 Jan 2014, Accepted 25 Jan 2014, Published online: 24 Feb 2014

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Fukutaro Mano, Stephen A. LoBue, Timothy W. Olsen, Alan D. Marmorstein & Jose S. Pulido. (2018) A novel missense mutation in BEST1 associated with an autosomal-dominant vitreoretinochoroidopathy (ADVIRC) phenotype. Ophthalmic Genetics 39:6, pages 749-753.
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Simone Kellner, Heidi Stöhr, Britta Fiebig, Silke Weinitz, Ghazaleh Farmand, Ulrich Kellner & Bernhard H. F. Weber. (2016) Fundus Autofluorescence and SD-OCT Document Rapid Progression in Autosomal Dominant Vitreoretinochoroidopathy (ADVIRC) Associated with a c.256G > A Mutation in BEST1. Ophthalmic Genetics 37:2, pages 201-208.
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Connie J. Chen, Stuart Kaufman, Kirk Packo, Heidi Stöhr, Bernhard H. F. Weber & Morton F. Goldberg. (2016) Long-Term Macular Changes in the First Proband of Autosomal Dominant Vitreoretinochoroidopathy (ADVIRC) Due to a Newly Identified Mutation in BEST1. Ophthalmic Genetics 37:1, pages 102-108.
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Articles from other publishers (1)

Elise Boulanger-ScemamaJose-Alain Sahel, Saddek Mohand-SaidAline AntonioChristel CondroyerChristina ZeitzIsabelle Audo. (2019) AUTOSOMAL DOMINANT VITREORETINOCHOROIDOPATHY. Retina 39:5, pages 867-878.
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