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

Ming-Yi Chung^{1

2}, Shih-Jen Chen³, Yun-Jin Jiang⁴

Affiliations

¹ Department of Life Sciences and Institute of Genome Sciences, National Yang Ming Chiao Tung University, Taipei, Taiwan.
² Department of Medical Research, Taipei Veterans General Hospital, Taipei, Taiwan.
³ Department of Ophthalmology, Taipei Veterans General Hospital, Taipei, Taiwan.
⁴ Institute of Molecular and Genomic Medicine, National Health Research Institutes, Miaoli County, Taiwan.

Comment

Ming-Yi Chung et al. Curr Eye Res. 2021 Dec.

. 2021 Dec;46(12):1931.

doi: 10.1080/02713683.2021.1924383. Epub 2021 Jun 14.

Ming-Yi Chung^{1

2}, Shih-Jen Chen³, Yun-Jin Jiang⁴

¹ Department of Life Sciences and Institute of Genome Sciences, National Yang Ming Chiao Tung University, Taipei, Taiwan.
² Department of Medical Research, Taipei Veterans General Hospital, Taipei, Taiwan.
³ Department of Ophthalmology, Taipei Veterans General Hospital, Taipei, Taiwan.
⁴ Institute of Molecular and Genomic Medicine, National Health Research Institutes, Miaoli County, Taiwan.

No abstract available

Comment in

Start and End with Genetics: RCBTB1 and Beyond.
Yang J, Sun W, Zhang Q. Yang J, et al. Curr Eye Res. 2021 Dec;46(12):1932-1933. doi: 10.1080/02713683.2021.1933060. Epub 2021 Jun 9. Curr Eye Res. 2021. PMID: 34011215

Variants in RCBTB1 are Associated with Autosomal Recessive Retinitis Pigmentosa but Not Autosomal Dominant FEVR.
Yang J, Xiao X, Sun W, Li S, Jia X, Zhang Q. Yang J, et al. Curr Eye Res. 2021 Jun;46(6):839-844. doi: 10.1080/02713683.2020.1842457. Epub 2020 Nov 18. Curr Eye Res. 2021. PMID: 33104391