Whole-exome screening for primary congenital glaucoma in Lebanon

Mutations were previously identified in the CYP1B1 gene in six out of 18 Lebanese families (33%) with primary congenital glaucoma (PCG). The purpose of this study is to determine the frequency and type of pathogenic mutations in other genes and compare to other populations using whole-exome sequenci...

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Bibliographische Detailangaben

Hauptverfasser:	Makhoul, Nadine J., Wehbi, Zahi, Hadi, Dalia El, Noureddine, Baha, Boustany, Rose-Mary, Al-Haddad, Christiane
Format:	Dataset
Sprache:	eng
Schlagworte:	Biological Sciences not elsewhere classified FOS: Biological sciences Genetics Microbiology Molecular Biology Virology
Online-Zugang:	Volltext bestellen
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