|
| Entrez Id: |
9896 |
| Gene Symbol: |
FIG4 |
FIG4
|
0.100 |
CausalMutation
|
phenotype |
CLINVAR |
Whole exome sequencing identifies three recessive FIG4-mutations in an apparently dominant pedigree with Charcot-Marie-Tooth disease.
|
25617005 |
2015 |
|
| Entrez Id: |
9896 |
| Gene Symbol: |
FIG4 |
FIG4
|
0.100 |
GeneticVariation
|
phenotype |
CLINVAR |
Whole exome sequencing identifies three recessive FIG4-mutations in an apparently dominant pedigree with Charcot-Marie-Tooth disease.
|
25617005 |
2015 |
|
| Entrez Id: |
9896 |
| Gene Symbol: |
FIG4 |
FIG4
|
0.100 |
GeneticVariation
|
phenotype |
CLINVAR |
Role of the phosphoinositide phosphatase FIG4 gene in familial epilepsy with polymicrogyria.
|
24598713 |
2014 |
|
| Entrez Id: |
9896 |
| Gene Symbol: |
FIG4 |
FIG4
|
0.100 |
CausalMutation
|
phenotype |
CLINVAR |
Role of the phosphoinositide phosphatase FIG4 gene in familial epilepsy with polymicrogyria.
|
24598713 |
2014 |
|
| Entrez Id: |
9896 |
| Gene Symbol: |
FIG4 |
FIG4
|
0.100 |
GeneticVariation
|
phenotype |
CLINVAR |
Yunis-Varón syndrome is caused by mutations in FIG4, encoding a phosphoinositide phosphatase.
|
23623387 |
2013 |
|
| Entrez Id: |
9896 |
| Gene Symbol: |
FIG4 |
FIG4
|
0.100 |
CausalMutation
|
phenotype |
CLINVAR |
Yunis-Varón syndrome is caused by mutations in FIG4, encoding a phosphoinositide phosphatase.
|
23623387 |
2013 |
|
| Entrez Id: |
9896 |
| Gene Symbol: |
FIG4 |
FIG4
|
0.100 |
GeneticVariation
|
phenotype |
CLINVAR |
Distinctive genetic and clinical features of CMT4J: a severe neuropathy caused by mutations in the PI(3,5)P₂ phosphatase FIG4.
|
21705420 |
2011 |
|
| Entrez Id: |
9896 |
| Gene Symbol: |
FIG4 |
FIG4
|
0.100 |
CausalMutation
|
phenotype |
CLINVAR |
Distinctive genetic and clinical features of CMT4J: a severe neuropathy caused by mutations in the PI(3,5)P₂ phosphatase FIG4.
|
21705420 |
2011 |
|
| Entrez Id: |
9896 |
| Gene Symbol: |
FIG4 |
FIG4
|
0.100 |
GeneticVariation
|
phenotype |
CLINVAR |
Deleterious variants of FIG4, a phosphoinositide phosphatase, in patients with ALS.
|
19118816 |
2009 |
|
| Entrez Id: |
9896 |
| Gene Symbol: |
FIG4 |
FIG4
|
0.100 |
CausalMutation
|
phenotype |
CLINVAR |
Deleterious variants of FIG4, a phosphoinositide phosphatase, in patients with ALS.
|
19118816 |
2009 |
|
| Entrez Id: |
9896 |
| Gene Symbol: |
FIG4 |
FIG4
|
0.100 |
GeneticVariation
|
phenotype |
CLINVAR |
Mutation of FIG4 causes neurodegeneration in the pale tremor mouse and patients with CMT4J.
|
17572665 |
2007 |
|
| Entrez Id: |
9896 |
| Gene Symbol: |
FIG4 |
FIG4
|
0.100 |
CausalMutation
|
phenotype |
CLINVAR |
Mutation of FIG4 causes neurodegeneration in the pale tremor mouse and patients with CMT4J.
|
17572665 |
2007 |
|
| Entrez Id: |
9896 |
| Gene Symbol: |
FIG4 |
FIG4
|
0.100 |
CausalMutation
|
phenotype |
CLINVAR |
Congenital heart malformation in Yunis-Varón syndrome.
|
8411078 |
1993 |
|
| Entrez Id: |
9896 |
| Gene Symbol: |
FIG4 |
FIG4
|
0.100 |
GeneticVariation
|
phenotype |
CLINVAR |
Congenital heart malformation in Yunis-Varón syndrome.
|
8411078 |
1993 |