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A Rare Case of Stargardt’s Disease Cover

A Rare Case of Stargardt’s Disease

Acta Medica Bulgarica
Volume 48 (2021): Issue 2 (July 2021)
By: I. Mermeklieva and  K. Kamenarova  
Open Access
|Aug 2021

Authors

I. Mermeklieva

elenamermeklieva@yahoo.com

Clinic of Ophthalmology, „Lozenetz“, University Hospital, Medical Faculty, University „Sv. Kliment Ohridski“, Sofia, Bulgaria

K. Kamenarova

Center of Molecular Medicine, Department of Medical Chemistry and Biochemistry, Medical University, Sofia, Bulgaria
DOI: https://doi.org/10.2478/amb-2021-0027 | Journal eISSN: 2719-5384 | Journal ISSN: 0324-1750
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Language: English
Page range: 76 - 80
Submitted on: Oct 5, 2020
|
Accepted on: Nov 20, 2020
|
Published on: Aug 11, 2021
Published by: Medical University - Sofia
In partnership with: Paradigm Publishing Services
Publication frequency: 4 issues per year
Keywords:
hereditary retinal dystrophy,
Stargardt’s disease,
electrophysiology,
genetics
Related subjects:
Medicine,
Basic medical science,
Immunology,
Clinical medicine,
Clinical medicine, other

© 2021 I. Mermeklieva, K. Kamenarova, published by Medical University - Sofia
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 License.

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