A commentary on the utility of a new L-DOPA-responsive dystonia mouse model.

Rare diseases (Austin, Tex.) Pub Date : 2015-12-29 eCollection Date: 2016-01-01 DOI:10.1080/21675511.2015.1128617
Samuel J Rose, Ellen J Hess
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Abstract

In a recent issue of Brain, we reported on the generation and characterization of a mouse model of the rare disease L-DOPA-responsive dystonia (DRD). Here, we discuss the utility of these mice for understanding broader disease processes and treatment strategies. Using specific experimental designs that either work "forward" from genetic etiology or "backward" from the symptomatic presentation, we discuss how our data and future work can be used to understand broader themes.

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一种新的左旋多巴反应性肌张力障碍小鼠模型的实用性评论。
在最近一期的《大脑》杂志上,我们报道了一种罕见疾病左旋多巴反应性肌张力障碍(DRD)的小鼠模型的产生和表征。在这里,我们讨论了这些小鼠在理解更广泛的疾病过程和治疗策略方面的效用。使用特定的实验设计,从遗传病因“向前”工作或从症状表现“向后”工作,我们讨论如何使用我们的数据和未来的工作来理解更广泛的主题。
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