Whole-exome screening for primary congenital glaucoma in Lebanon.
Nadine J MakhoulZahi WehbiDalia El HadiBaha NoureddineRose-Mary BoustanyChristiane Al-HaddadPublished in: Ophthalmic genetics (2023)
This study provides new data on the spectrum of mutations of PCG in Lebanon. This highlights the genetic heterogeneity of the Lebanese population, noted for high rates of consanguinity in 50% in this cohort. This study emphasizes the importance of whole-exome sequencing in elucidating new candidate genes for PCG in the Lebanese.