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

Curr Eye Res. 2021 Dec;46(12):1931. doi: 10.1080/02713683.2021.1924383. Epub 2021 Jun 14.

Authors

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.

PMID: 34126825
DOI: 10.1080/02713683.2021.1924383

No abstract available

Publication types

Letter
Comment

MeSH terms

Familial Exudative Vitreoretinopathies
Fluorescein Angiography
Guanine Nucleotide Exchange Factors / genetics
Humans
Phenotype
Retinal Diseases* / diagnosis
Retinal Diseases* / genetics

Substances

Guanine Nucleotide Exchange Factors
RCBTB1 protein, human