Mutations in ATOH7 gene in patients with nonsyndromic congenital retinal nonattachment and familial exudative vitreoretinopathy-Reference-Cited by-同舟云学术

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Mutations in ATOH7 gene in patients with nonsyndromic congenital retinal nonattachment and familial exudative vitreoretinopathy

Published:2016-03-02 Issue:4 Volume:37 Page:462-464
ISSN:1381-6810
Container-title:Ophthalmic Genetics
language:en
Short-container-title:Ophthalmic Genetics

Author:

Kondo Hiroyuki¹²,Matsushita Itsuka¹,Tahira Tomoko³,Uchio Eiichi²,Kusaka Shunji⁴

Affiliation:

1. Department of Ophthalmology, University of Occupational and Environmental Health, Japan, Kitakyushu, Japan

2. Department of Ophthalmology, Fukuoka University, Fukuoka, Japan

3. Innovation Center for Medical Redox Navigation, Kyushu University, Kyushu, Japan

4. Department of Ophthalmology, Sakai Hospital, Kinki University Faculty of Medicine, Sakai, Japan

Funder

Japan Society for the Promotion of Science

Publisher

Informa UK Limited

Subject

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

Link

https://www.tandfonline.com/doi/pdf/10.3109/13816810.2015.1120316

Reference11 articles.

1. Heterogeneity of Congenital Retinal Non-Attachment, Falciform Folds and Retinal Dysplasia

2. Deletion of a remote enhancer near ATOH7 disrupts retinal neurogenesis, causing NCRNA disease

3. High incidence of autosomal recessive nonsyndromal congenital retinal nonattachment (NCRNA) in an Iranian founding population

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1. Identification and Characterization of ATOH7-Regulated Target Genes and Pathways in Human Neuroretinal Development;Cells;2024-07-03

2. Next-generation sequencing to genetically diagnose a diverse range of inherited eye disorders in 15 consanguineous families from Pakistan;Experimental Eye Research;2024-07

3. Multimodal imaging of white preretinal lesions in atypical familial exudative vitreoretinopathy: Case report and literature review;American Journal of Ophthalmology Case Reports;2024-06

4. Clinical and genetic characteristics and natural history of Finnish families with familial exudative vitreoretinopathy due to pathogenic FZD4 variants;Acta Ophthalmologica;2024-05-05

5. Deciphering a crucial dimeric interface governing Norrin dimerization and the pathogenesis of familial exudative vitreoretinopathy;The FASEB Journal;2024-02-16

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