Mapping and Cloning - Leber Congenital Amaurosis

Stockton, David W.

Abstract

Funding Agency

• Agency: National Institute of Health (NIH)
• Institute: National Eye Institute (NEI)
• Type: Mentored Patient-Oriented Research Career Development Award (K23)
• Project #: 5K23EY000375-05
• Application #: 6384230
• Study Section: Special Emphasis Panel (ZEY1-VSN (04))
• Program Officer: Dudley, Peter A
• Project Start: 1997-08-01
• Project End: 2002-07-31
• Budget Start: 2001-08-01
• Budget End: 2002-07-31
• Support Year: 5
• Fiscal Year: 2001
• Total Cost: $128,556

Institution

• Name: Baylor College of Medicine
• Department: Genetics
• Type: Schools of Medicine
• DUNS #: 051113330
• City: Houston
• State: TX
• Country: United States
• Zip Code: 77030

Publications

Bejjani, B A; Stockton, D W; Lewis, R A et al. (2000) Multiple CYP1B1 mutations and incomplete penetrance in an inbred population segregating primary congenital glaucoma suggest frequent de novo events and a dominant modifier locus. Hum Mol Genet 9:367-74