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Successive neuron loss in the thalamus and cortex in a mouse model of infantile neuronal ceroid lipofuscinosis

✍ Scribed by Catherine Kielar; Lucy Maddox; Ellen Bible; Charlie C. Pontikis; Shannon L. Macauley; Megan A. Griffey; Michael Wong; Mark S. Sands; Jonathan D. Cooper

Book ID
113812093
Publisher
Elsevier Science
Year
2007
Tongue
English
Weight
966 KB
Volume
25
Category
Article
ISSN
0969-9961

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## Abstract The neuronal ceroid lipofuscinoses (NCLs) are a family of devastating pediatric neurodegenerative disorders and currently represent the most common form of pediatric‐onset neurodegeneration. Infantile NCL (INCL), the most aggressive of these disorders, is caused by mutations in the __CL