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Common variants in the COL2A1 gene are associated with lattice degeneration of the retina in a Japanese population
PURPOSE: Lattice degeneration of the retina is a vitreoretinal disorder characterized by a visible fundus lesion that predisposes the patient to retinal detachment. It has been suggested that collagen type II alpha 1 (COL2A1) gene variants may contribute to the development of disorders associated wi...
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| Publicado no: | Mol Vis |
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| Main Authors: | , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Molecular Vision
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6925665/ https://ncbi.nlm.nih.gov/pubmed/31908402 |
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