Neuronal Ceroid Lipofuscinoses Are Connected at Molecular Level: Interaction of CLN5 Protein with CLN2 and CLN3

Neuronal ceroid lipofuscinoses (NCLs) are neurodegenerative storage diseases characterized by mental retardation, visual failure, and brain atrophy as well as accumulation of storage material in multiple cell types. The diseases are caused by mutations in the ubiquitously expressed genes, of which s...

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Pubblicato in:	Mol Biol Cell
Autori principali:	Vesa, Jouni, Chin, Mark H., Oelgeschläger, Kathrin, Isosomppi, Juha, DellAngelica, Esteban C., Jalanko, Anu, Peltonen, Leena
Natura:	Artigo
Lingua:	Inglês
Pubblicazione:	American Society for Cell Biology 2002
Soggetti:	Article
Accesso online:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC117323/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/12134079/ https://ncbi.nlm.nih.govhttps://doi.org/10.1091/mbc.E02-01-0031
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