Pupillary Light Reflex Deficits in a Canine Model of Late Infantile Neuronal Ceroid Lipofuscinosis

Late-infantile neuronal ceroid lipofuscinosis (CLN2) is a hereditary neurological disorder characterized by progressive retinal degeneration and vision loss, cognitive and motor decline, seizures, and pronounced brain atrophy. The progressive loss of neurological functions eventually leads to death,...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: Whiting, Rebecca E.H., Narfström, Kristina, Yao, Gang, Pearce, Jacqueline W., Coates, Joan R., Castaner, Leilani J., Katz, Martin L.
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: 2013
Pynciau:
Article
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC3845481/
https://ncbi.nlm.nih.gov/pubmed/24135299
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.exer.2013.10.006
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