A Novel Mutation in the FYCO1 Gene Causing Congenital Cataract: Case Study of a Chinese Family

Congenital cataract is the most important global cause of visual impairment in children. Autosomal dominant and autosomal recessive inheritance account for the majority of the hereditary nonsyndromic congenital cataract. The function of FYCO1 gene is to guide the transport of the microtubule-directe...

Descripción completa

Detalles Bibliográficos
Autores principales: Mei, Shuping, Lin, Jingwei, Liu, Zhen, Li, Cheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2022
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9439885/
https://www.ncbi.nlm.nih.gov/pubmed/36061348
http://dx.doi.org/10.1155/2022/5838104

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9439885/
https://www.ncbi.nlm.nih.gov/pubmed/36061348
http://dx.doi.org/10.1155/2022/5838104

Ejemplares similares