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Genetically modified rodent models of Spinocerebellar Ataxia Type 17

Spinocerebellar ataxia type 17 (SCA17) is a family member of Autosomal Dominant Cerebellar Ataxias (ADCA) characterized by variable manifestations, including cerebellar ataxia, dementia and psychiatric symptoms. Since the identification of a CAG repeat expansion in the TBP gene in a patient with ata...

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Bibliografiska uppgifter
I publikationen:J Neurosci Res
Huvudupphovsmän: Cui, Yiting, Yang, Su, Li, Xiao-Jiang, Li, Shihua
Materialtyp: Artigo
Språk:Inglês
Publicerad: 2016
Ämnen:
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC5508981/
https://ncbi.nlm.nih.gov/pubmed/27859490
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/jnr.23984
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