Novel retinal findings in peroxisomal biogenesis disorders-Reference-Cited by-同舟云学术

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Novel retinal findings in peroxisomal biogenesis disorders

Published:2018-01-29 Issue:3 Volume:39 Page:377-379
ISSN:1381-6810
Container-title:Ophthalmic Genetics
language:en
Short-container-title:Ophthalmic Genetics

Author:

O’Bryhim B. E.¹,Kozel B. A.²³,Lueder G. T.¹⁴

Affiliation:

1. Department of Ophthalmology and Visual Sciences, Washington University in St. Louis, St. Louis, MO, USA

2. Department of Pediatrics, Washington University School of Medicine, St. Louis, MO, USA

3. National Institutes of Health, National Heart, Lung, and Blood Institute, Bethesda, MD, USA

4. Department of Pediatrics, St. Louis Children’s Hospital, St. Louis, MO, USA

Publisher

Informa UK Limited

Subject

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

Link

https://www.tandfonline.com/doi/pdf/10.1080/13816810.2018.1430241

Reference8 articles.

1. Peroxisome biogenesis disorders in the Zellweger spectrum: An overview of current diagnosis, clinical manifestations, and treatment guidelines

2. The peroxisome and the eye

3. Leopard spot retinal pigmentation in infancy indicating a peroxisomal disorder

4. Peroxisomal bifunctional enzyme deficiency with associated retinal findings

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Characterization of Severity in Zellweger Spectrum Disorder by Clinical Findings: A Scoping Review, Meta-Analysis and Medical Chart Review;Cells;2022-06-10

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