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Ophthalmic Genetics Volume 42, 2021 - Issue 1
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Case Reports

Ophthalmic findings and a novel CTC1 gene mutation in coats plus syndrome: a case report

Tingyi LiangDepartment of Ophthalmology, Xinhua Hospital, Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai, ChinaView further author information
,
Xiang ZhangDepartment of Ophthalmology, Xinhua Hospital, Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai, ChinaView further author information
,
Yu XuDepartment of Ophthalmology, Xinhua Hospital, Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai, ChinaCorrespondence[email protected]
View further author information
&
Peiquan ZhaoDepartment of Ophthalmology, Xinhua Hospital, Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai, ChinaCorrespondence[email protected]
View further author information
Pages 79-83 | Received 16 Jul 2020, Accepted 10 Sep 2020, Published online: 09 Oct 2020

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Ashley López-Cañizares, Maria P. Fernandez, Hasenin Al-Khersan, Piero Carletti, Monica S Arroyo, Maria C Fernandez-Ruiz & Audina M Berrocal. (2022) Coats plus in prematurity. Ophthalmic Genetics 43:4, pages 543-549.
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Articles from other publishers (5)

Rishi Kumar Jaiswal, Kai-Hang Lei, Megan Chastain, Yuan Wang, Olga Shiva, Shan Li, Zhongsheng You, Peter Chi & Weihang Chai. (2023) CaMKK2 and CHK1 phosphorylate human STN1 in response to replication stress to protect stalled forks from aberrant resection. Nature Communications 14:1.
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Fae B. Kayarian, Steven M. Cohen, Mark L. Cohen & Daniel E. Sammartino. (2023) Coats Plus Syndrome Presenting in an Adult. Journal of VitreoRetinal Diseases 7:6, pages 562-564.
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Avery E. Sears, Caroline C. Awh, Shafeeque Kunhiabdullah, Jonathan E. Sears & Danny A. Mammo. (2022) Coats Plus Syndrome in a Premature Infant, With a Focus on Management. Journal of VitreoRetinal Diseases 7:1, pages 74-78.
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Weihang Chai, Megan Chastain, Olga Shiva & Yuan Wang. (2021) The Intrinsically Disordered Region in the Human STN1 OB-Fold Domain Is Important for Protecting Genome Stability. Biology 10:10, pages 977.
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Hiroyuki Kondo, Itsuka Matsushita, Tatsuo Nagata, Etsuko Fujihara, Katsuhiro Hosono, Eiichi Uchio, Yoshihiro Hotta & Shunji Kusaka. (2021) Retinal Features of Family Members With Familial Exudative Vitreoretinopathy Caused By Mutations in KIF11 Gene . Translational Vision Science & Technology 10:7, pages 18.
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