CLINICAL CHARACTERISTICS OF OCCULT MACULAR DYSTROPHY IN FAMILY WITH MUTATION OF RP1L1 GENE-Reference-Cited by-同舟云学术

CLINICAL CHARACTERISTICS OF OCCULT MACULAR DYSTROPHY IN FAMILY WITH MUTATION OF RP1L1 GENE

Published:2012-06 Issue:6 Volume:32 Page:1135-1147
ISSN:0275-004X
Container-title:Retina
language:en
Short-container-title:

Author:

Tsunoda Kazushige,Usui Tomoaki,Hatase Tetsuhisa,Yamai Satoshi,Fujinami Kaoru,Hanazono Gen,Shinoda Kei,Ohde Hisao,Akahori Masakazu,Iwata Takeshi,Miyake Yozo

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Ophthalmology,General Medicine

Reference27 articles.

1. Hereditary macular dystrophy without visible fundus abnormality.;Miyake;Am J Ophthalmol,1989

2. . Occult macular dystrophy.;Miyake;Am J Ophthalmol,1996

3. . Multifocal electroretinography in patients with occult macular dystrophy.;Fujii;Br J Ophthalmol,1999

4. . Multifocal electroretinogram in occult macular dystrophy.;Piao;Invest Ophthalmol Vis Sci,2000

5. Multifocal electroretinogram (mfERG) in a family with occult macular dystrophy (OMD).;Wildberger;Klin Monatsbl Augenheilkd,2003

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