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Ophthalmic Genetics Volume 37, 2016 - Issue 4
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Letters to the Journal

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

Hiroyuki KondoDepartment of Ophthalmology, University of Occupational and Environmental Health, Japan, Kitakyushu, Japan;Department of Ophthalmology, Fukuoka University, Fukuoka, JapanCorrespondence[email protected]
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,
Itsuka MatsushitaDepartment of Ophthalmology, University of Occupational and Environmental Health, Japan, Kitakyushu, JapanView further author information
,
Tomoko TahiraInnovation Center for Medical Redox Navigation, Kyushu University, Kyushu, JapanView further author information
,
Eiichi UchioDepartment of Ophthalmology, Fukuoka University, Fukuoka, JapanView further author information
&
Shunji KusakaDepartment of Ophthalmology, Sakai Hospital, Kinki University Faculty of Medicine, Sakai, JapanView further author information
Pages 462-464 | Published online: 02 Mar 2016

Citations (10)

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Toshiaki Asano, Kazuma Oku & Hiroyuki Kondo. (2021) Familial exudative vitreoretinopathy with TGFBR2 mutation without signs of Loeys-Dietz syndrome. Ophthalmic Genetics 42:5, pages 637-640.
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Articles from other publishers (9)

Sho Naruse & Hiroyuki Kondo. (2023) OCULAR FEATURES ASSOCIATED WITH MUTATIONS IN ATOH7 GENE OVERLAP THOSE WITH FAMILIAL EXUDATIVE VITREORETINOPATHY. RETINAL Cases & Brief Reports 17:6, pages 694-698.
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David Atac, Lucas Mohn, Silke Feil, Kevin Maggi, Dominik Haenni, Britta Seebauer, Samuel Koller & Wolfgang Berger. (2022) Functional Characterization of an In-Frame Deletion in the Basic Domain of the Retinal Transcription Factor ATOH7. International Journal of Molecular Sciences 23:3, pages 1053.
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Justin Brodie-Kommit, Brian S. Clark, Qing ShiFion Shiau, Dong Won Kim, Jennifer LangelCatherine Sheely, Philip A Ruzycki, Michel FriesAwais Javed, Michel Cayouette, Tiffany Schmidt, Tudor Badea, Tom Glaser, Haiqing ZhaoJoshua Singer, Seth Blackshaw & Samer Hattar. (2021) Atoh7-independent specification of retinal ganglion cell identity. Science Advances 7:11.
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Sankaranarayanan Rajkumar, Vidya Gopinathan Nair & Abhay Raghukant Vasavada. 2021. Advances in Vision Research, Volume III. Advances in Vision Research, Volume III 329 363 .
Shane D'Souza & Richard A. Lang. (2020) Retinal ganglion cell interactions shape the developing mammalian visual system. Development 147:23.
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Giuseppina Covello, Fernando J. Rossello, Michele Filosi, Felipe Gajardo, Anne‐Laure Duchemin, Beatrice F. Tremonti, Michael Eichenlaub, Jose M. Polo, David Powell, John Ngai, Miguel L. Allende, Enrico Domenici, Mirana Ramialison & Lucia Poggi. (2020) Transcriptome analysis of the zebrafish atoh7−/− Mutant, lakritz , highlights Atoh7‐dependent genetic networks with potential implications for human eye diseases . FASEB BioAdvances 2:7, pages 434-448.
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Huijuan Xu, Shanshan Zhang, Lulin Huang, Peiquan Zhao, Xiang Zhang, Zhenglin Yang & Lin Zhang. (2020) Identification of novel variants in the FZD4 gene associated with familial exudative vitreoretinopathy in Chinese families . Clinical & Experimental Ophthalmology 48:3, pages 356-365.
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J. Plaisancié, F. Ceroni, R. Holt, C. Zazo Seco, P. Calvas, N. Chassaing & Nicola K. Ragge. (2019) Genetics of anophthalmia and microphthalmia. Part 1: Non-syndromic anophthalmia/microphthalmia. Human Genetics 138:8-9, pages 799-830.
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Dyah W Karjosukarso, Sebastianus H C van Gestel, Jieqiong Qu, Evelyn N Kouwenhoven, Lonneke Duijkers, Alejandro Garanto, Huiqing Zhou & Rob W J Collin. (2018) An FEVR-associated mutation in ZNF408 alters the expression of genes involved in the development of vasculature. Human Molecular Genetics 27:20, pages 3519-3527.
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