ETIOPATHOGENETIC FEATURE OF STARGHARDT DISEASE. THE OPPORTUNITIES OF CLINICAL AND MOLECULAR GENETIC DIAGNOSIS (LITERATURE REVIEW)
Starghardt macular dystrophy is one of the most common hereditary macular dystrophies. ABCR gene has a high level of polymorphism, multiple pathological mutations and difficult feature of inheritance. All these factors determine the special methods of clinical and molecular genetic diagnosis.
| Main Authors: | , , |
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| Format: | Article |
| Language: | Russian |
| Published: |
Publishing house "Ophthalmology"
2015-12-01
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| Series: | Офтальмохирургия |
| Subjects: | |
| Online Access: | https://www.ophthalmosurgery.ru/jour/article/view/141 |