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The Ophthalmic Genetics and Visual Function Branch (OGVFB) / Ophthalmic Molecular Genetics Section (OMGS) is involved in a number of different approaches to the study inherited diseases affecting the visual system.
One approach to understanding inherited visual diseases uses principles of positional cloning to identify genes important in human Mendelian inherited diseases. Such diseases currently undergoing linkage analysis, gene isolation, or characterization of mutations include retinitis pigmentosa, inherited cataracts, glaucoma, and a number of corneal dystrophies.
A second approach is to attempt to establish associations between DNA sequence changes in or near candidate genes and specific phenotypes. This type of study is most applicable to common diseases with a complex inheritance pattern, and is currently being used for age-related cataracts, primary open angle glaucoma, and high myopia.
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论文共 241 篇作者统计合作学者相似作者
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Journal of Translational Medicineno. 1 (2024): 1-18
Investigative Ophthalmology & Visual Scienceno. 4 (2023): 29-29
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Journal of glaucomano. 7 (2023): E80-E89
Biochemistryno. 12 (2023): 1864-1877
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Investigative ophthalmology & visual scienceno. 4 (2023): 29
Venkata Pulla Rao Vendra, Christian Ostrowski, Marzena A. Dyba,Sergey G. Tarasov,J. Fielding Hejtmancik
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCESno. 18 (2023)
BRITISH JOURNAL OF OPHTHALMOLOGYpp.bjo-322673, (2023)
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