Identification and Functional Characterization of Mutation in FYCO1 in Families with Congenital Cataract

Congenital cataract (CC) causes a third of the cases of treatable childhood blindness worldwide. CC is a disorder of the crystalline lens which is established as clinically divergent and has complex heterogeneity. This study aimed to determine the genetic basis of CC. Whole blood was obtained from f...

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Detalles Bibliográficos
Autores principales: Ullah, Muhammad Ikram, Rehman, Zaira, Dad, Rubina, Alsrhani, Abdullah, Shakil, Muhammad, Ghanem, Heba Bassiony, Alameen, Ayman Ali Mohammed, Elsadek, Mohamed Farouk, Eltayeb, Lienda Bashier, Ullah, Sajjad, Atif, Muhammad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10456301/
https://www.ncbi.nlm.nih.gov/pubmed/37629644
http://dx.doi.org/10.3390/life13081788

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10456301/
https://www.ncbi.nlm.nih.gov/pubmed/37629644
http://dx.doi.org/10.3390/life13081788

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