AUTOSOMAL DOMINANT MÜLLER CELL SHEEN DYSTROPHY-Reference-Cited by-同舟云学术

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AUTOSOMAL DOMINANT MÜLLER CELL SHEEN DYSTROPHY

Published:2022-05 Issue:5 Volume:42 Page:981-991
ISSN:0275-004X
Container-title:Retina
language:en
Short-container-title:

Author:

Dalma-Weiszhausz José,Chacón-Camacho Oscar,CHEVEZ-BARRIOS Patricia,Zenteno Juan C.,Franco-Cárdenas Valentina,García-Montaño Leopoldo A.,Pérez-Bravo Jehieli,García-Montalvo Iván A.,Jiménez-Sierra Juan M.,Dalma Alexander

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Ophthalmology,General Medicine

Reference33 articles.

1. Autosomal dominant lateonset cellophane-likesheen vitreomacular dystrophy: a new entity;Dalma;Invest Ophthalmol Vis Sci,1991

2. Familial internal limiting membrane dystrophy: a new sheen retinal dystrophy;Polk;Arch Ophthalmol,1997

3. Electrophysiological evaluation of visual loss in Müller cell sheen dystrophy;Kellner;Br J Ophthalmol,1998

4. Standard for clinical electroretinography;Marmor;Arch Ophthalmol,1989

5. Exome sequencing identifies a SREBF1 recurrent ARG557CYS mutation as the cause of hereditary mucoepithelial dysplasia in a family with high clinical variability;Chacón-Camacho;Am J Med Genet A,2020

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