Novel Likely Pathogenic Variants Identified by Panel-Based Exome Sequencing in Congenital Cataract Patients

PURPOSE: To identify likely pathogenic variants in three families with congenital cataracts via panel-based exome sequencing. METHODS: A panel containing 153 genes associated with congenital cataracts was designed. Genes were selected through reference to databases including the Human Gene Mutation...

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Detalles Bibliográficos
Autores principales: Chen, Doudou, Yang, Tao, Zhu, Siquan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2021
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8612798/
https://www.ncbi.nlm.nih.gov/pubmed/34840822
http://dx.doi.org/10.1155/2021/3847409

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8612798/
https://www.ncbi.nlm.nih.gov/pubmed/34840822
http://dx.doi.org/10.1155/2021/3847409

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