遗传突变的视紫红质，光传感蛋白的燃料棒细胞，单是最常见的一种形式的反相和大多数这些突变导致蛋白质错误折叠。
Inherited mutations in rhodopsin, the light sensing protein of rods cells, are the single most common cause of one form of RP and the majority of these mutations cause protein misfolding.
Blue Gene/L 技术提供了一种强大的方法来研究这些类型的疾病，因为它能够更加经济高效地（和更快地）建模蛋白质折叠和错误折叠的效果。
The Blue Gene/L technology offers a powerful way to study these types of diseases, because it provides a more cost-effective (and faster) way to model the effects of protein folding and misfolding.
学习蛋白质折叠式了解一些神经性能疾病的关键，而这些疾病则是由于某些蛋白质的折叠错误而产生的。
Studying protein folding is key to understanding several neurodegenerative diseases that are a result of the incorrect folding of certain protein strings.
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