PHOTORECEPTOR INNER SEGMENT MORPHOLOGY IN BEST VITELLIFORM MACULAR DYSTROPHY-Reference-Cited by-同舟云学术

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PHOTORECEPTOR INNER SEGMENT MORPHOLOGY IN BEST VITELLIFORM MACULAR DYSTROPHY

Published:2017-04 Issue:4 Volume:37 Page:741-748
ISSN:0275-004X
Container-title:Retina
language:en
Short-container-title:

Author:

Scoles Drew,Sulai Yusufu N.,Cooper Robert F.,Higgins Brian P.,Johnson Ryan D.,Carroll Joseph,Dubra Alfredo,Stepien Kimberly E.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Ophthalmology,General Medicine

Reference36 articles.

1. Best's vitelliform dystrophy;Blodi;Ophthalmic Paediatr Genet,1990

2. Autosomal recessive bestrophinopathy: differential diagnosis and treatment options;Boon;Ophthalmology,2013

3. Identification of the gene responsible for Best macular dystrophy;Petrukhin;Nat Genet,1998

4. Genetic linkage of vitelliform macular degeneration (Best's disease) to chromosome 11q13;Stone;Nat Genet,1992

5. Bestrophin, the product of the Best vitelliform macular dystrophy gene (VMD2), localizes to the basolateral plasma membrane of the retinal pigment epithelium;Marmorstein;Proc Natl Acad Sci U S A,2000

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