Cargando…
FZD4 in a Large Chinese Population With Familial Exudative Vitreoretinopathy: Molecular Characteristics and Clinical Manifestations
PURPOSE: The purpose of this study was to establish a genotype-phenotype correlation of familial exudative vitreoretinopathy (FEVR) caused by FZD4 gene mutations. METHODS: Six hundred fifty-one probands and their family members were recruited based on a clinical diagnosis of FEVR between 2015 and 20...
Autores principales: | Lu, Jinglin, Huang, Li, Sun, Limei, Li, Songshan, Zhang, Zhaotian, Jiang, Zhaoxin, Li, Jiaqing, Ding, Xiaoyan |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Association for Research in Vision and Ophthalmology
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8994167/ https://www.ncbi.nlm.nih.gov/pubmed/35394490 http://dx.doi.org/10.1167/iovs.63.4.7 |
Ejemplares similares
-
Whole-Gene Deletions of FZD4 Cause Familial Exudative Vitreoretinopathy
por: Huang, Li, et al.
Publicado: (2021) -
Familial Exudative Vitreoretinopathy and Systemic Abnormalities in Patients With CTNNB1 Mutations
por: Huang, Li, et al.
Publicado: (2023) -
Identification of Five Novel Variants in the TSPAN12 Gene in Chinese Families With Familial Exudative Vitreoretinopathy
por: Wang, You, et al.
Publicado: (2023) -
Novel mutations in FZD4 and phenotype–genotype correlation in Chinese patients with familial exudative vitreoretinopathy
por: Tang, Miao, et al.
Publicado: (2016) -
Quantitative Analysis of Vascular Abnormalities in Full-Term Infants With Mild Familial Exudative Vitreoretinopathy
por: Li, Peng, et al.
Publicado: (2023)