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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Detalles Bibliográficos
Autores principales: Okazaki, Shinya, Meguro, Akira, Ideta, Ryuichi, Takeuchi, Masaki, Yonemoto, Junichi, Teshigawara, Takeshi, Yamane, Takahiro, Okada, Eiichi, Ideta, Hidenao, Mizuki, Nobuhisa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Vision 2019
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6925665/
https://www.ncbi.nlm.nih.gov/pubmed/31908402

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6925665/
https://www.ncbi.nlm.nih.gov/pubmed/31908402

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