×
Entrez Id:
54982
Gene Symbol:
CLN6
CLN6
0.590
Biomarker
disease
MGD
Neuronal ceroid lipofuscinosis (nclf), a new disorder of the mouse linked to chromosome 9.
9600738
1998
×
Entrez Id:
54982
Gene Symbol:
CLN6
CLN6
0.590
GeneticVariation
disease
BEFREE
CLN6 , the gene for a variant late infantile neuronal ceroid lipofuscinosis , has been mapped to chromosome 15q21-23 by homozygosity mapping.
10191123
1999
×
Entrez Id:
54982
Gene Symbol:
CLN6
CLN6
0.590
GeneticVariation
disease
BEFREE
A survey of fibroblasts and lymphoblasts demonstrated that lack of activity was associated with LINCL arising from mutations in the CLN2 gene but not other neuronal ceroid lipofuscinoses (NCLs), including the CLN6 variant LINCL , classical infantile NCL, classical juvenile NCL, and adult NCL (Kufs' disease).
10428067
1999
×
Entrez Id:
54982
Gene Symbol:
CLN6
CLN6
0.590
GeneticVariation
disease
BEFREE
CLN6 , the gene for variant late infantile neuronal ceroid lipofuscinosis , was mapped to a 4 cM region on chromosome 15q22-23.
11589002
2001
×
Entrez Id:
54982
Gene Symbol:
CLN6
CLN6
0.590
GeneticVariation
disease
BEFREE
Novel mutations in the CLN6 gene causing a variant late infantile neuronal ceroid lipofuscinosis .
12673792
2003
×
Entrez Id:
54982
Gene Symbol:
CLN6
CLN6
0.590
GeneticVariation
disease
BEFREE
Spectrum of CLN6 mutations in variant late infantile neuronal ceroid lipofuscinosis .
12815591
2003
×
Entrez Id:
54982
Gene Symbol:
CLN6
CLN6
0.590
GeneticVariation
disease
BEFREE
Variant late infantile neuronal ceroid lipofuscinosis (CLN6 gene) in Saudi Arabia.
19520283
2009
×
Entrez Id:
54982
Gene Symbol:
CLN6
CLN6
0.590
GeneticVariation
disease
BEFREE
A relatively inexpensive CLN6 mutation screening should be considered first in Morocco as an initial diagnosis step when the disease course is consistent with late infantile neuronal ceroid-lipofuscinosis .
23180398
2013
×
Entrez Id:
54982
Gene Symbol:
CLN6
CLN6
0.590
Biomarker
disease
CTD_human
Altered biometal homeostasis is associated with CLN6 mRNA loss in mouse neuronal ceroid lipofuscinosis.
23789114
2013
×
Entrez Id:
54982
Gene Symbol:
CLN6
CLN6
0.590
GeneticVariation
disease
BEFREE
A first CLN6 variant case of late infantile neuronal ceroid lipofuscinosis caused by a homozygous mutation in a boy from China: a case report.
30285654
2018
×
Entrez Id:
54982
Gene Symbol:
CLN6
CLN6
0.590
GeneticVariation
disease
BEFREE
Mutations in CLN6 cause late-infantile neuronal ceroid lipofuscinosis (LINCL ), and teenage and adult onset NCL without visual impairment.
30528883
2019