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CLN6 gene

Known as: HsT18960, ceroid-lipofuscinosis, neuronal 6, late infantile, variant, FLJ20561 
National Institutes of Health

Related topics

Related topics

1 relation
CEROID LIPOFUSCINOSIS, NEURONAL, 6

Papers overview

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2015
2015
Expression und Proteinwechselwirkungen von murinem Cln6 und seine Rolle in der Pathogenese der Neuronalen Ceroid Lipofuszinosen
2009
2009
A new strategy to identify the disease causing mutation for neuronal ceroid lipofuscinosis in South Hamsphire sheep.
The New Zealand South Hampshire sheep have been well characterised as an animal model for variant late-infantile neuronal ceroid… 
2006
2006
A Genome-wide Scan Maps a Novel Juvenile-Onset Primary Open-Angle Glaucoma Locus to 15 q
METHODS. A complete ophthalmic examination was conducted, and genomic DNA was obtained from 25 members of a Chinese family, of… 
2001
2001
Analysis of candidate genes in the CLN6 critical region using in silico cloning.
CLN6, the gene for variant late infantile neuronal ceroid lipofuscinosis, was mapped to a 4 cM region on chromosome 15q22-23… 
2001
2001
In Silico Cloning: the identification of genes within the CLN6 critical region.
2001
2001
Analysis of candidate genes in the CLN6 using in silico cloning critical region
1999
1999
Progress toward positional cloning of ovine neuronal ceroid lipofuscinosis, a model of the human late-infantile variant CLN6.
The neuronal ceroid lipofuscinoses (NCLs) are lysosomal storage diseases with severe neurodegenerative pathology. An ovine model… 
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