Decrease of FZD4 exon 1 methylation in probands from FZD4-associated FEVR family of phenotypic heterogeneity

Familial exudative vitreoretinopathy (FEVR) is an important cause of childhood blindness and is clinically characterized by phenotypic heterogeneity. FEVR patients harboring the same genetic mutation vary widely in disease severity. The purpose of this study was to explore non-genetic factors that r...

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Detalles Bibliográficos
Autores principales: Liu, Miaomiao, Luo, Jia, Feng, Huazhang, Li, Jing, Zhang, Xiang, Zhao, Peiquan, Fei, Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Medicine
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9638120/
https://www.ncbi.nlm.nih.gov/pubmed/36353221
http://dx.doi.org/10.3389/fmed.2022.976520

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9638120/
https://www.ncbi.nlm.nih.gov/pubmed/36353221
http://dx.doi.org/10.3389/fmed.2022.976520

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