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Updated: May 6, 2026

A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations
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A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations

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在补体调节器CD55促进器区域的21-bp删除与多焦点运动神经病变及其疾病过程有关

Jeroen W Bos1, Ewout J N Groen1, Henny G Otten2

  • 1Department of Neurology and Neurosurgery, UMC Utrecht Brain Center, Utrecht University, Utrecht, The Netherlands.

Journal of the peripheral nervous system : JPNS
|March 26, 2024
PubMed
概括

一种特定的CD55基因删除 (rs2871582) 与多焦点运动神经病变 (MMN) 易感性和更有利的疾病过程有关. 这一发现突显了补体系统在MMN免疫病理学中的作用.

关键词:
CD55 CD55 CD55 CD55 CD55 CD55 CD55 CD55 CD55 CD55 CD55 CD55 CD55 CD55 CD55 CD55 CD55 CD55在DAF中,我们得到了DAF的支持.互补系统是互补的系统.遗传学 遗传学 遗传学 是一个多焦点运动神经病变.

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In Vivo Electrophysiological Measurement of Compound Muscle Action Potential from the Forelimbs in Mouse Models of Motor Neuron Degeneration06:35

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