Molecular Genetics of Primary Congenital Glaucoma and Juvenile Open Angle Glaucoma

Author:

Rezaie T.,Walter M.A.

Publisher

Elsevier

Reference33 articles.

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

2. FOXC1 transcriptional regulation is mediated by N- and C-terminal activation domains and contains a phosphorylated transcriptional inhibitory domain;Berry;J. Biol. Chem.,2002

3. Peters anomaly: review of the literature;Bhandari;Cornea,2011

4. Gln48His is the prevalent myocilin mutation in primary open angle and primary congenital glaucoma phenotypes in India;Chakrabarti;Mol. Vis.,2005

5. Analysis of CYP1B1 gene mutations in patients with primary congenital glaucoma;Chouiter;J. Pediatr. Genet.,2017

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