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MOLECULAR-GENETICS OF RETINITIS-PIGMENTOSA
Author(s): DRYJA TP, LI T
Source: HUMAN MOLECULAR GENETICS    Volume: 4    Special Issue: Sp. Iss. SI    Pages: 1739-1743    Published: 1995  
Times Cited: 201     References: 85     
Abstract: Hereditary degenerations and dysfunctions of the retina are an extremely heterogeneous group of diseases. This summary deals with recent advances in the molecular genetics of a subset of those disorders, namely, those encompassed under the diagnosis 'retinitis pigmentosa'. Over 20 loci where mutations cause retinitis pigmentosa have been mapped; the review focuses on the seven retinitis pigmentosa loci that have been identified.
Document Type: Review
Language: English
Reprint Address: DRYJA, TP (reprint author), HARVARD UNIV, MASSACHUSETTS EYE & EAR INFIRM, SCH MED, OCULAR MOLEC GENET LAB, BOSTON, MA 02114 USA
Addresses:
1. HARVARD UNIV, MASSACHUSETTS EYE & EAR INFIRM, SCH MED, BERMAN GUND LAB STUDY RETINAL DEGENERAT, BOSTON, MA 02114 USA
Publisher: OXFORD UNIV PRESS UNITED KINGDOM, WALTON ST JOURNALS DEPT, OXFORD, ENGLAND OX2 6DP
Subject Category: Biochemistry & Molecular Biology; Genetics & Heredity
IDS Number: TC033
ISSN: 0964-6906
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