Short Report: Prevalence of CYP1B1 mutations in Australian patients with primary congenital glaucoma

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...

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Veröffentlicht in:	Clinical genetics 2007-09, Vol.72 (3), p.255
Hauptverfasser:	Dimasi, D P, Hewitt, A W, Straga, T, Pater, J, MacKinnon, J R, Elder, JE, Casey, T, Mackey, DA, JE, Craig
Format:	Artikel
Sprache:	eng
Schlagworte:	Deoxyribonucleic acid DNA Genetics Genomics Glaucoma Mutation
Online-Zugang:	Volltext
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