Article
Prevalence of CYP1B1 mutations in Australian patients with primary congenital glaucoma
7 Aug 2007
Abstract excerpt
Analysis of CYP1B1 in primary congenital glaucoma (PCG) patients from various ethnic populations indicates that allelic heterogeneity is high, and some mutations are population specific. No study has previously reported the rate or spectrum of CYP1B1 mutations in Australian PCG patients. The aim of this study is to determine the frequency of CYP1B1 mutations in our predominately Caucasian, Australian cohort of...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
