Colocalization of neuronal ceroid lipofuscinosis proteins suggests a common pathway involved in embryonic and adult neurogenesis
The neuronal ceroid lipofuscinoses (NCLs) are a family of neurodegenerative diseases predominantly affecting infants and children, which in some cases can present into adulthood. There are fourteen genes comprising the 13 known subtypes of NCLs (CLN1-CLN8, CLN10-CLN14; CLN9 has been reclassified as...
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| Language: | en_US |
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2021
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| Online Access: | https://hdl.handle.net/2144/43463 |