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Mutation of the Stargardt disease gene (ABCR) in age-related macular degeneration
Author(s): Allikmets R, Shroyer NF, Singh N, Seddon JM, Lewis RA, Bernstein PS, Peiffer A, Zabriskie NA, Li YX, Hutchinson A, Dean M, Lupski JR, Leppert M
Source: SCIENCE    Volume: 277    Issue: 5333    Pages: 1805-1807    Published: SEP 19 1997  
Times Cited: 436     References: 25     
Abstract: Age-related macular degeneration (AMD) is the leading cause of severe central visual impairment among the elderly and is associated both with environmental factors such as smoking and with genetic factors. Here, 167 unrelated AMD patients were screened for alterations in ABCR, a gene that encodes a retinal rod photoreceptor protein and is defective in Stargardt disease, a common hereditary form of macular dystrophy. Thirteen different AMD-associated alterations, both deletions and amino acid substitutions, were found in one allele of ABCR in 26 patients (16%). Identification of ABCR alterations will permit presymptomatic testing of high-risk individuals and may lead to earlier diagnosis of AMD and to new strategies for prevention and therapy.
Document Type: Article
Language: English
Addresses:
1. NCI, LAB GENOM DIVERS, FREDERICK CANC RES & DEV CTR, FREDERICK, MD 21702 USA
2. NCI, INTRAMURAL RES SUPPORT PROGRAM, SAIC FREDERICK, FREDERICK CANC RES & DEV CTR, FREDERICK, MD 21702 USA
3. BAYLOR COLL MED, DEPT MOL & HUMAN GENET, HOUSTON, TX 77030 USA
4. UNIV UTAH, DEPT HUMAN GENET, ECCLED INST HUMAN GENET, SALT LAKE CITY, UT 84112 USA
5. HARVARD UNIV, MASSACHUSETTS EYE & EAR INFIRM, SCH MED, DEPT OPHTHALMOL, BOSTON, MA 02114 USA
6. BAYLOR COLL MED, DEPT OPHTHALMOL, HOUSTON, TX 77030 USA
7. BAYLOR COLL MED, DEPT PEDIAT, HOUSTON, TX 77030 USA
8. BAYLOR COLL MED, DEPT MED, HOUSTON, TX 77030 USA
9. UNIV UTAH, MORAN EYE CTR, DEPT OPHTHALMOL, SALT LAKE CITY, UT 84132 USA
Publisher: AMER ASSOC ADVANCEMENT SCIENCE, 1200 NEW YORK AVE, NW, WASHINGTON, DC 20005
Subject Category: Multidisciplinary Sciences
IDS Number: XX298
ISSN: 0036-8075
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