Case Report: A de novo Variant of CRYGC Gene Associated With Congenital Cataract and Microphthalmia

Background: Congenital cataract is one of the most common causes of blindness in children. A rapid and accurate genetic diagnosis benefit the patients in the pediatric department. The current study aims to identify the genetic defects in a congenital cataract patient without a family history. Case p...

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Detalles Bibliográficos
Autores principales: Peng, Yu, Zheng, Yu, Deng, Zifeng, Zhang, Shuju, Tan, Yilan, Hu, Zhengmao, Tao, Lijuan, Luo, Yulin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9198712/
https://www.ncbi.nlm.nih.gov/pubmed/35719371
http://dx.doi.org/10.3389/fgene.2022.866246

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9198712/
https://www.ncbi.nlm.nih.gov/pubmed/35719371
http://dx.doi.org/10.3389/fgene.2022.866246

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