GLUT1 DEFICIENCY SYNDROME 1
|
0.700 |
GeneticVariation
|
disease |
UNIPROT |
Mutations in Disordered Regions Can Cause Disease by Creating Dileucine Motifs.
|
30197081 |
2018 |
GLUT1 DEFICIENCY SYNDROME 1
|
0.700 |
Biomarker
|
disease |
CLINGEN |
Gene therapy for a mouse model of glucose transporter-1 deficiency syndrome.
|
28119822 |
2017 |
GLUT1 DEFICIENCY SYNDROME 1
|
0.700 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
Advantages and pitfalls of an extended gene panel for investigating complex neurometabolic phenotypes.
|
27604308 |
2016 |
GLUT1 DEFICIENCY SYNDROME 1
|
0.700 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
A 23 years follow-up study identifies GLUT1 deficiency syndrome initially diagnosed as complicated hereditary spastic paraplegia.
|
27725288 |
2016 |
GLUT1 DEFICIENCY SYNDROME 1
|
0.700 |
GeneticVariation
|
disease |
UNIPROT |
A Protein Kinase C Phosphorylation Motif in GLUT1 Affects Glucose Transport and is Mutated in GLUT1 Deficiency Syndrome.
|
25982116 |
2015 |
GLUT1 DEFICIENCY SYNDROME 1
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
Nationwide survey of glucose transporter-1 deficiency syndrome (GLUT-1DS) in Japan.
|
25487684 |
2015 |
GLUT1 DEFICIENCY SYNDROME 1
|
0.700 |
Biomarker
|
disease |
CLINGEN |
From splitting GLUT1 deficiency syndromes to overlapping phenotypes.
|
26193382 |
2015 |
GLUT1 DEFICIENCY SYNDROME 1
|
0.700 |
GeneticVariation
|
disease |
UNIPROT |
Crystal structure of the human glucose transporter GLUT1.
|
24847886 |
2014 |
GLUT1 DEFICIENCY SYNDROME 1
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
Clinical utility of genetic testing in pediatric drug-resistant epilepsy: a pilot study.
|
25108116 |
2014 |
GLUT1 DEFICIENCY SYNDROME 1
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
Unusual sensitivity to steroid treatment in intractable childhood epilepsy suggests GLUT1 deficiency syndrome.
|
22976442 |
2012 |
GLUT1 DEFICIENCY SYNDROME 1
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
Glucose transporter 1 deficiency as a treatable cause of myoclonic astatic epilepsy.
|
21555602 |
2011 |
GLUT1 DEFICIENCY SYNDROME 1
|
0.700 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
Paroxysmal choreoathetosis/spasticity (DYT9) is caused by a GLUT1 defect.
|
21832227 |
2011 |
GLUT1 DEFICIENCY SYNDROME 1
|
0.700 |
GeneticVariation
|
disease |
UNIPROT |
Glucose transporter-1 deficiency syndrome: the expanding clinical and genetic spectrum of a treatable disorder.
|
20129935 |
2010 |
GLUT1 DEFICIENCY SYNDROME 1
|
0.700 |
GeneticVariation
|
disease |
UNIPROT |
Absence epilepsies with widely variable onset are a key feature of familial GLUT1 deficiency.
|
20574033 |
2010 |
GLUT1 DEFICIENCY SYNDROME 1
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
Early-onset absence epilepsy caused by mutations in the glucose transporter GLUT1.
|
19798636 |
2009 |
GLUT1 DEFICIENCY SYNDROME 1
|
0.700 |
GeneticVariation
|
disease |
UNIPROT |
Autosomal recessive inheritance of GLUT1 deficiency syndrome.
|
20221955 |
2009 |
GLUT1 DEFICIENCY SYNDROME 1
|
0.700 |
GeneticVariation
|
disease |
UNIPROT |
Childhood chorea with cerebral hypotrophy: a treatable GLUT1 energy failure syndrome.
|
19901175 |
2009 |
GLUT1 DEFICIENCY SYNDROME 1
|
0.700 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
Paroxysmal exercise-induced dyskinesia and epilepsy is due to mutations in SLC2A1, encoding the glucose transporter GLUT1.
|
18577546 |
2008 |
GLUT1 DEFICIENCY SYNDROME 1
|
0.700 |
Biomarker
|
disease |
CLINGEN |
GLUT1 mutations are a cause of paroxysmal exertion-induced dyskinesias and induce hemolytic anemia by a cation leak.
|
18451999 |
2008 |
GLUT1 DEFICIENCY SYNDROME 1
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
Disease-associated Glut1 single amino acid substitute mutations S66F, R126C, and T295M constitute Glut1-deficiency states in vitro.
|
17052934 |
2007 |
GLUT1 DEFICIENCY SYNDROME 1
|
0.700 |
Biomarker
|
disease |
CLINGEN |
A mouse model for Glut-1 haploinsufficiency.
|
16497725 |
2006 |
GLUT1 DEFICIENCY SYNDROME 1
|
0.700 |
GeneticVariation
|
disease |
UNIPROT |
Glut-1 deficiency syndrome: clinical, genetic, and therapeutic aspects.
|
15622525 |
2005 |
GLUT1 DEFICIENCY SYNDROME 1
|
0.700 |
GeneticVariation
|
disease |
UNIPROT |
Imaging the metabolic footprint of Glut1 deficiency on the brain.
|
12325075 |
2002 |
GLUT1 DEFICIENCY SYNDROME 1
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
Imaging the metabolic footprint of Glut1 deficiency on the brain.
|
12325075 |
2002 |
GLUT1 DEFICIENCY SYNDROME 1
|
0.700 |
GeneticVariation
|
disease |
UNIPROT |
Autosomal dominant glut-1 deficiency syndrome and familial epilepsy.
|
11603379 |
2001 |