Localization of juvenile, but not late-infantile, neuronal ceroid lipofuscinosis on chromosome 16.

The neuronal ceroid lipofuscinoses (NCL) are a group of progressive neurodegenerative disorders characterized by the deposition of autofluorescent proteinaceous fingerprint or curvilinear bodies. We have found that CLN3, the gene underlying the juvenile form of NCL, is very tightly linked to the din...

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Hlavní autoři: Yan, W, Boustany, R M, Konradi, C, Ozelius, L, Lerner, T, Trofatter, J A, Julier, C, Breakefield, X O, Gusella, J F, Haines, J L
Médium: Artigo
Jazyk:Inglês
Vydáno: 1993
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Research Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1682098/
https://ncbi.nlm.nih.gov/pubmed/8434611
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