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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Détails bibliographiques
Auteurs principaux: von Schantz, Carina, Kielar, Catherine, Hansen, Stine N, Pontikis, Charlie C, Alexander, Noreen A, Kopra, Outi, Jalanko, Anu, Cooper, Jonathan D
Format: Artigo
Langue:Inglês
Publié: 2009
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Article
Accès en ligne: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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