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

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 loci such a...

Ausführliche Beschreibung

Gespeichert in:

Bibliographische Detailangaben
Veröffentlicht in:	Egyptian Journal of Medical Human Genetics 2021-09, Vol.22 (1), p.73-11, Article 73
Hauptverfasser:	Ng, Ker Hsin, Subrayan, Visvaraja, Ramachandran, Vasudevan, Ismail, Fazliana
Format:	Artikel
Sprache:	eng
Schlagworte:	Analysis Chromosome 14 Cornea Corneal dystrophy Endothelial corneal dystrophy Endothelium Fuchs Genes Genetic aspects Genetic diversity Genetic polymorphism Health aspects Illumina Information management Medical research Medicine Medicine & Public Health Medicine, Experimental Pathophysiology Single nucleotide polymorphisms Single-nucleotide polymorphism
Online-Zugang:	Volltext
Tags:	Tag hinzufügen Keine Tags, Fügen Sie den ersten Tag hinzu!

Schreiben Sie den ersten Kommentar!