Genetics in primary congenital glaucoma: Implications in disease management and counseling

Author:

Leysen L.,Cassiman C.,Vermeer S.ORCID,Casteels I.,Balikova I.

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics,General Medicine

Reference78 articles.

1. Screening of CYP1B1 and LTBP2 genes in Saudi families with primary congenital glaucoma: genotype-phenotype correlation;Abu-Amero;Mol. Vis.,2011

2. Genotype/phenotype correlation in primary congenital glaucoma patients in the Lebanese population: a pilot study;Al-Haddad;Ophthalmic Genet.,2016

3. The loss of microglia activities facilitates glaucoma progression in association with CYP1B1 gene mutation (p.Gly61Glu);Alghamdi;PLoS One,2020

4. Null mutations in LTBP2 cause primary congenital glaucoma;Ali;Am. J. Hum. Genet.,2009

5. Congenital glaucoma and CYP1B1: an old story revisited;Alsaif;Hum. Genet.,2019

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