早产儿严重视网膜病变中TSPAN12和KIF11基因的突变 - Suppr | 超能文献

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Mutations in TSPAN12 gene causing familial exudative vitreoretinopathy.TSPAN12 基因突变导致家族性渗出性玻璃体视网膜病变。

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本文引用的文献

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A Review on the Incidence and Related Risk Factors of Retinopathy of Prematurity Across Various Countries.各国早产儿视网膜病变的发病率及相关危险因素综述

Cureus. 2022 Nov 29;14(11):e32007. doi: 10.7759/cureus.32007. eCollection 2022 Nov.

2

Retinopathy of prematurity: contribution of inflammatory and genetic factors.早产儿视网膜病变：炎症和遗传因素的作用

Mol Cell Biochem. 2022 Jun;477(6):1739-1763. doi: 10.1007/s11010-022-04394-4. Epub 2022 Mar 9.

3

Endothelial nitric oxide synthase G894T, intron 4 VNTR, and T786C polymorphisms in retinopathy of prematurity.