CYP1B1 copy number variation is not a major contributor to primary congenital glaucoma

CYP1B1 copy number variation is not a major contributor to primary congenital glaucoma

Purpose: To evaluate the prevalence and the diagnostic utility of testing for CYP1B1 copy number variation (CNV) in primary congenital glaucoma (PCG) cases unexplained by CYP1B1 point mutations in The Australian and New Zealand Registry of Advanced Glaucoma.

Bibliographic Details
Main Authors: Souzeau, Emmanuelle, Hayes, Melanie, Ruddle, Jonathan B., Elder, James E., Staffieri, Sandra E., Kearns, Lisa S., Mackey, David A., Zhou, Tiger, Ridge, Bronwyn, Burdon, Kathryn P., Dubowsky, Andrew, Craig, Jamie E.
Format: Online
Language:English
Published: Molecular Vision 2015
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4333725/

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4333725/

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