Screening of single nucleotide polymorphisms among fuchs’ endothelial corneal dystrophy subjects in Malaysia

Screening of single nucleotide polymorphisms among fuchs’ endothelial corneal dystrophy subjects in Malaysia

Abstract Background The pathophysiology underlying Fuchs' Endothelial Corneal Dystrophy (FECD), especially in older individuals, remains unclear, with a genetic predisposition being reported as the single best predictor of the disease. Genetic studies have shown that several genes in various lo...

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Bibliographic Details
Main Authors: Ker Hsin Ng, Visvaraja Subrayan, Vasudevan Ramachandran, Fazliana Ismail
Format: Article
Language:English
Published: SpringerOpen 2021-09-01
Series:Egyptian Journal of Medical Human Genetics
Subjects:
Genetic polymorphism
Illumina
Fuchs
Endothelial corneal dystrophy
Online Access:https://doi.org/10.1186/s43042-021-00193-6

Internet

https://doi.org/10.1186/s43042-021-00193-6

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