MERTK missense variants in three patients with retinitis pigmentosa-Reference-Cited by-同舟云学术

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MERTK missense variants in three patients with retinitis pigmentosa

Published:2022-08-29 Issue:1 Volume:44 Page:74-82
ISSN:1381-6810
Container-title:Ophthalmic Genetics
language:en
Short-container-title:Ophthalmic Genetics

Author:

Poli Federica E.¹²^ORCID,Yusuf Imran H.¹²,Clouston Penny³,Shanks Morag³,Whitfield Jennifer³,Charbel Issa Peter¹²,MacLaren Robert E.¹²

Affiliation:

1. Nuffield Laboratory of Ophthalmology, Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford, UK

2. Oxford Eye Hospital, Oxford University Hospitals NHS Foundation Trust, Oxford, UK

3. Oxford Regional Genetics Laboratories, Oxford University Hospitals NHS Foundation Trust, Oxford, UK

Funder

National Institute for Health Research

Publisher

Informa UK Limited

Subject

Genetics (clinical),Ophthalmology,Pediatrics, Perinatology and Child Health

Link

https://www.tandfonline.com/doi/pdf/10.1080/13816810.2022.2113541

Reference40 articles.

1. Retinitis pigmentosa

2. RetNet: summaries of genes and loci causing retinal diseases. 2021. https://sph.uth.edu/retnet/sum-dis.htm#A-genes.

3. Non-syndromic retinitis pigmentosa

4. Mertk Triggers Uptake of Photoreceptor Outer Segments during Phagocytosis by Cultured Retinal Pigment Epithelial Cells

5. Biology of the TAM Receptors

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2. Challenges and Opportunities in the Genetic Analysis of Inherited Retinal Dystrophies in Africa, a Literature Review;Journal of Personalized Medicine;2023-01-29

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