Conclusion Construction of the eukaryotic expression vectors of wild type and mutant PRPF31 genes is basic work for research on the mechanisms of retinitis pigmentosa caused by PRPF31 mutation.

结论野生型和突变型PRPF31基因真核表达载体的构建，为研究PRPF31基因突变引起视网膜色素变性的机制奠定了基础。

Therefore, we believe that some of these drugs could be developed as potential treatments to delay or prevent blindness in rhodopsin retinitis pigmentosa patients.

因此，我们认为，这些药物可能发展成为潜在的治疗方法，延误或阻止失明的视紫红质视网膜色素变性病人。

Objective to investigate the characteristics of the multifocal electroretinogram (ERG) and to evaluate the application values of the multifocal ERG in retinitis pigmentosa (RP).

目的研究视网膜色素变性(RP)的多焦视网膜电图(erg)特性和评价多焦erg应用价值。

Within the decade, she says, therapies involving similar eye genes could improve sight in people with other mutations, such as retinitis pigmentosa or macular degeneration.

她表示，十年内利用类似的治疗方法可以改善与其他基因突变有关的视力问题，如视网膜色素变性和黄斑变性。

Objective to identify the disease locus in X - linked retinitis pigmentosa (XLRP) families using genetic linkage analysis.

目的应用遗传连锁分析方法对X连锁型视网膜色素变性家系进行分析，确定其致病基因的所在位点。

It also marks the first step toward the development of transplant-ready retinas to treat eye disorders such as retinitis pigmentosa and macular degeneration that affect millions.

此项成果也标志着移植用视网膜的开发向前迈出了第一步，后者将成为数百万罹患视网膜色素变性、黄斑变性等眼疾的患者的福音。

Conclusion Intraocular lens implantation can help to improve the visual acuity of most patients with cataract complicated retinitis pigmentosa and is an effective and safe treatment method.

结论白内障人工晶状体植入术对大部分视网膜色素变性并发白内障患者的视力提高有帮助，是一种较为安全有效的治疗方法。

More about retinitis pigmentosa and current research threads can be found in the 「about RP」 and 「research」 sections of this site.

更多关于视网膜色素变性和目前的研究线索中可以找到「关于反相」和「研究」节本网站。

Objective to detect mutations of the RP2 gene in two Chinese families with X linked retinitis pigmentosa (XLRP).

目的检测引起2个家系产生X连锁视网膜色素变性的RP2基因突变。