Neurodevelopmental delay in the Cln3(Δex7/8) mouse model for Batten disease

Juvenile neuronal ceroid lipofuscinosis (JNCL), also known as Batten disease, is a fatal inherited neurodegenerative disorder. The major clinical features of this disease are vision loss, seizures and progressive cognitive and motor decline starting in childhood. Mutations in CLN3 are known to cause...

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Detaylı Bibliyografya
Asıl Yazarlar: Osório, Nuno S., Sampaio-Marques, Belém, Chan, Chun-Hung, Oliveira, Pedro, Pearce, David A., Sousa, Nuno, Rodrigues, Fernando
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2009
Konular:
Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC3114406/
https://ncbi.nlm.nih.gov/pubmed/19243453
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1601-183X.2009.00478.x
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