Retinal Degeneration In A Mouse Model Of CLN5 Disease Is Associated With Compromised Autophagy

The Finnish variant of late infantile neuronal ceroid lipofuscinosis (CLN5 disease) belongs to a family of neuronal ceroid lipofuscinosis (NCLs) diseases. Vision loss is among the first clinical signs in childhood forms of NCLs. Mutations in CLN5 underlie CLN5 disease. The aim of this study was to c...

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Publicado no:Sci Rep
Main Authors: Leinonen, Henri, Keksa-Goldsteine, Velta, Ragauskas, Symantas, Kohlmann, Philip, Singh, Yajuvinder, Savchenko, Ekaterina, Puranen, Jooseppi, Malm, Tarja, Kalesnykas, Giedrius, Koistinaho, Jari, Tanila, Heikki, Kanninen, Katja M.
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group UK 2017
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5431647/
https://ncbi.nlm.nih.gov/pubmed/28487519
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-017-01716-1
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