Disease Modeling with Human Neurons Reveals LMNB1 Dysregulation Underlying DYT1 Dystonia

DYT1 dystonia is a hereditary neurologic movement disorder characterized by uncontrollable muscle contractions. It is caused by a heterozygous mutation in Torsin A (TOR1A), a gene encoding a membrane-embedded ATPase. While animal models provide insights into disease mechanisms, significant species-d...

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Detaylı Bibliyografya
Yayımlandı:J Neurosci
Asıl Yazarlar: Ding, Baojin, Tang, Yu, Ma, Shuaipeng, Akter, Masuma, Liu, Meng-Lu, Zang, Tong, Zhang, Chun-Li
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Society for Neuroscience 2021
Konular:
Research Articles
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC7939088/
https://ncbi.nlm.nih.gov/pubmed/33468570
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.2507-20.2020
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