Progressive thalamocortical neuron loss in Cln5 deficient mice: distinct effects in Finnish variant late infantile NCL

Finnish variant LINCL (vLINCL(Fin)) is the result of mutations in the CLN5 gene. To gain insights into the pathological staging of this fatal pediatric disorder, we have undertaken a stereological analysis of the CNS of Cln5 deficient mice (Cln5(-/-)) at different stages of disease progression. Cons...

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Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: von Schantz, Carina, Kielar, Catherine, Hansen, Stine N, Pontikis, Charlie C, Alexander, Noreen A, Kopra, Outi, Jalanko, Anu, Cooper, Jonathan D
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: 2009
Gaiak:
Article
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC2704904/
https://ncbi.nlm.nih.gov/pubmed/19385065
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.nbd.2009.02.001
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