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在加油站付出代价:钠钾ATP酶突变导致的肌张力障碍

Paying the price at the pump: dystonia from mutations in a Na+/K+ -ATPase.

作者信息

Cannon Stephen C

机构信息

Department of Neurology, UT Southwestern Medical Center at Dallas, TX 75390, USA.

出版信息

Neuron. 2004 Jul 22;43(2):153-4. doi: 10.1016/j.neuron.2004.07.002.

Abstract

Dystonia is a disorder of involuntary sustained muscle contraction, which usually affects a focal region of the body but may be generalized and results in twisting contorted movements or abnormal postures. Several clinical subtypes of dystonia have been delineated and many have a strong inherited basis. In this issue of Neuron, de Carvalho Aguiar and colleagues report the identification of missense mutations in the gene for the Na+/K+ -ATPase alpha3 subunit (ATP1A3) as a cause of rapid-onset dystonia-parkinsonism (RDP, DYT12).

摘要

肌张力障碍是一种非自主性持续肌肉收缩的疾病,通常影响身体的一个局部区域,但也可能全身性发作,导致扭曲变形的动作或异常姿势。肌张力障碍已被划分为几种临床亚型,其中许多都有很强的遗传基础。在本期《神经元》杂志中,德·卡瓦略·阿吉亚尔及其同事报告称,已鉴定出钠钾ATP酶α3亚基(ATP1A3)基因中的错义突变是快速发作性肌张力障碍-帕金森综合征(RDP,DYT12)的病因。

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