|
| Entrez Id: |
2896 |
| Gene Symbol: |
GRN |
GRN
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
Clinical and genetic analyses of familial and sporadic frontotemporal dementia patients in Southern Italy.
|
28264768 |
2017 |
|
| Entrez Id: |
2896 |
| Gene Symbol: |
GRN |
GRN
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
A Novel Splice-Acceptor Site Mutation in GRN (c.709-2 A>T) Causes Frontotemporal Dementia Spectrum in a Large Family from Southern Italy.
|
27258413 |
2016 |
|
| Entrez Id: |
2896 |
| Gene Symbol: |
GRN |
GRN
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
Distinct clinical characteristics of C9orf72 expansion carriers compared with GRN, MAPT, and nonmutation carriers in a Flanders-Belgian FTLD cohort.
|
23338682 |
2013 |
|
| Entrez Id: |
2896 |
| Gene Symbol: |
GRN |
GRN
|
0.700 |
GeneticVariation
|
disease |
CLINVAR |
Strikingly different clinicopathological phenotypes determined by progranulin-mutation dosage.
|
22608501 |
2012 |
|
| Entrez Id: |
2896 |
| Gene Symbol: |
GRN |
GRN
|
0.700 |
GermlineCausalMutation
|
disease |
ORPHANET |
Strikingly different clinicopathological phenotypes determined by progranulin-mutation dosage.
|
22608501 |
2012 |
|
| Entrez Id: |
2896 |
| Gene Symbol: |
GRN |
GRN
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
Serum progranulin levels in patients with frontotemporal lobar degeneration and Alzheimer's disease: detection of GRN mutations in a Spanish cohort.
|
22647257 |
2012 |
|
| Entrez Id: |
2896 |
| Gene Symbol: |
GRN |
GRN
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
Strikingly different clinicopathological phenotypes determined by progranulin-mutation dosage.
|
22608501 |
2012 |
|
| Entrez Id: |
2896 |
| Gene Symbol: |
GRN |
GRN
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
Genetic and clinical features of progranulin-associated frontotemporal lobar degeneration.
|
21482928 |
2011 |
|
| Entrez Id: |
2896 |
| Gene Symbol: |
GRN |
GRN
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
The spectrum of mutations in progranulin: a collaborative study screening 545 cases of neurodegeneration.
|
20142524 |
2010 |
|
| Entrez Id: |
2896 |
| Gene Symbol: |
GRN |
GRN
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
Molecular characterization of novel progranulin (GRN) mutations in frontotemporal dementia.
|
18183624 |
2008 |
|
| Entrez Id: |
2896 |
| Gene Symbol: |
GRN |
GRN
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
Clinicopathologic features of frontotemporal dementia with progranulin sequence variation.
|
17202431 |
2007 |
|
| Entrez Id: |
2896 |
| Gene Symbol: |
GRN |
GRN
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
Neuropathologic heterogeneity in HDDD1: a familial frontotemporal lobar degeneration with ubiquitin-positive inclusions and progranulin mutation.
|
17334266 |
2007 |
|
| Entrez Id: |
2896 |
| Gene Symbol: |
GRN |
GRN
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
A novel progranulin mutation associated with variable clinical presentation and tau, TDP43 and alpha-synuclein pathology.
|
17439980 |
2007 |
|
| Entrez Id: |
2896 |
| Gene Symbol: |
GRN |
GRN
|
0.700 |
GeneticVariation
|
disease |
CLINVAR |
Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration.
|
16950801 |
2006 |
|
| Entrez Id: |
2896 |
| Gene Symbol: |
GRN |
GRN
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration.
|
16950801 |
2006 |
|
| Entrez Id: |
2896 |
| Gene Symbol: |
GRN |
GRN
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17.
|
16862116 |
2006 |
|
| Entrez Id: |
2896 |
| Gene Symbol: |
GRN |
GRN
|
0.700 |
GeneticVariation
|
disease |
CLINVAR |
Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17.
|
16862116 |
2006 |
|
| Entrez Id: |
2896 |
| Gene Symbol: |
GRN |
GRN
|
0.700 |
Biomarker
|
disease |
CTD_human |
|
|
|
|
| Entrez Id: |
2896 |
| Gene Symbol: |
GRN |
GRN
|
0.700 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
|
|
|