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Cerebellar contribution to the cognitive alterations in SCA1: evidence from mouse models

Spinocerebellar ataxia type 1 (SCA1) is a fatal neurodegenerative disease caused by abnormal expansion of glutamine (Q) encoding CAG repeats in the gene Ataxin-1 (ATXN1). Although motor and balance deficits are the core symptoms of SCA1, cognitive decline is also commonly observed in patients. While...

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Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:Hum Mol Genet
Egile Nagusiak: Asher, Melissa, Rosa, Juao-Guilherme, Rainwater, Orion, Duvick, Lisa, Bennyworth, Michael, Lai, Ruo-Yah, Kuo, Sheng-Han, Cvetanovic, Marija
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Oxford University Press 2019
Gaiak:
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC8216071/
https://ncbi.nlm.nih.gov/pubmed/31696233
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddz265
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