Stargardt disease: monitoring incidence and diagnostic trends in the Netherlands using a nationwide disease registry-Reference-Cited by-同舟云学术

Stargardt disease: monitoring incidence and diagnostic trends in the Netherlands using a nationwide disease registry

Published:2021-08-25 Issue: Volume: Page:
ISSN:1755-375X
Container-title:Acta Ophthalmologica
language:en
Short-container-title:Acta Ophthalmol

Author:

Runhart Esmee H.¹²^ORCID,Dhooge Patty¹²^ORCID,Meester‐Smoor Magda³,Pas Jeroen¹,Pott Jan Willem R.⁴,Leeuwen Redmer⁵,Kroes Hester Y.⁶,Bergen Arthur A.⁷⁸,Jong‐Hesse Yvonne⁹,Thiadens Alberta A.³,Schooneveld Mary J.⁹¹⁰,Genderen Maria⁵¹⁰,Boon Camiel⁹¹¹,Klaver Caroline¹³¹²,den Born L. Ingeborg¹³¹⁴,Cremers Frans P. M.²¹⁵^ORCID,Hoyng Carel B.¹²^ORCID

Affiliation:

1. Department of Ophthalmology Radboud University Medical Centre Nijmegen the Netherlands

2. Donders Institute for Brain Cognition and Behaviour Radboud University Medical Centre Nijmegen the Netherlands

3. Department of Ophthalmology Erasmus University Medical Centre Rotterdam the Netherlands

4. Department of Ophthalmology University Medical Centre Groningen University of Groningen Groningen the Netherlands

5. Department of Ophthalmology University Medical Centre Utrecht Utrecht the Netherlands

6. Department of Genetics University Medical Centre Utrecht Utrecht the Netherlands

7. Department of Clinical Genetics Academic Medical Centre Amsterdam the Netherlands

8. The Netherlands Institute for Neuroscience (NIN‐KNAW) Amsterdam the Netherlands

9. Department of Ophthalmology Amsterdam University Medical Centres Amsterdam the Netherlands

10. Bartiméus Diagnostic Centre for Complex Visual Disorders Zeist the Netherlands

11. Department of Ophthalmology Leiden University Medical Centre Leiden the Netherlands

12. Department of Epidemiology Erasmus University Medical Centre Rotterdam the Netherlands

13. The Rotterdam Eye Hospital Rotterdam the Netherlands

14. Rotterdam Ophthalmic Institute Rotterdam the Netherlands

15. Department of Human Genetics Radboud University Medical Centre Nijmegen the Netherlands

Publisher

Wiley

Subject

Ophthalmology,General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/aos.14996

Reference33 articles.

1. A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Starqardt macular dystrophy

2. Future of Rare Diseases Research 2017-2027: An IRDiRC Perspective

3. The Problem of Rarity: Estimation of Prevalence in Rare Disease

4. In SilicoFunctional Meta-Analysis of 5,962ABCA4Variants in 3,928 Retinal Dystrophy Cases

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