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Current Eye Research Volume 46, 2021 - Issue 12
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Letters to Editor

Phenotype Variability in the Patients of Familial Exudative Vitreoretinopathy: the RCBTB1 case

Ming-yi Chunga Department of Life Sciences and Institute of Genome Sciences, National Yang Ming Chiao Tung University, Taipei, Taiwan;b Department of Medical Research, Taipei Veterans General Hospital, Taipei, TaiwanCorrespondence[email protected]
ORCID Iconhttps://orcid.org/0000-0003-2198-6860
ORCID Icon,
Shih-Jen Chenc Department of Ophthalmology, Taipei Veterans General Hospital, Taipei, TaiwanORCID Iconhttps://orcid.org/0000-0001-9798-1578
ORCID Icon &
Yun-Jin Jiangd Institute of Molecular and Genomic Medicine, National Health Research Institutes, Miaoli County, TaiwanORCID Iconhttps://orcid.org/0000-0003-0499-7306
ORCID Icon
Page 1931 | Received 01 Dec 2020, Accepted 01 Apr 2021, Published online: 14 Jun 2021

Citations (2)

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Read on this site (1)

Junxing Yang, Wenmin Sun & Qingjiong Zhang. (2021) Start and End with Genetics: RCBTB1 and Beyond. Current Eye Research 46:12, pages 1932-1933.
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Articles from other publishers (1)

Handong Dan, Dongdong Wang, Zixu Huang, Qianqian Shi, Miao Zheng, Yuanyuan Xiao & Zongming Song. (2022) Whole exome sequencing revealed 14 variants in NDP, FZD4, LRP5, and TSPAN12 genes for 20 families with familial exudative vitreoretinopathy. BMC Medical Genomics 15:1.
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