Identification and Functional Characterization of Mutation in <i>FYCO1</i> in Families with Congenital Cataract

Identification and Functional Characterization of Mutation in <i>FYCO1</i> 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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Bibliographic Details
Main Authors: Muhammad Ikram Ullah, Zaira Rehman, Rubina Dad, Abdullah Alsrhani, Muhammad Shakil, Heba Bassiony Ghanem, Ayman Ali Mohammed Alameen, Mohamed Farouk Elsadek, Lienda Bashier Eltayeb, Sajjad Ullah, Muhammad Atif
Format: Article
Language:English
Published: MDPI AG 2023-08-01
Series:Life
Subjects:
congenital cataract
<i>FYCO1</i>
mutations
consanguineous families
in silico analysis
Online Access:https://www.mdpi.com/2075-1729/13/8/1788

Internet

https://www.mdpi.com/2075-1729/13/8/1788

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