rs1064795935
|
|
Movement Disorders
|
T |
0.700 |
GeneticVariation
|
CLINVAR |
High-throughput genetic characterization of a cohort of Brugada syndrome patients.
|
26220970 |
2015 |
rs1064795935
|
|
Movement Disorders
|
T |
0.700 |
GeneticVariation
|
CLINVAR |
Variants of anterior segment dysgenesis and cerebral involvement in a large family with a novel COL4A1 mutation.
|
23394911 |
2013 |
rs1064795935
|
|
Movement Disorders
|
T |
0.700 |
GeneticVariation
|
CLINVAR |
Novel COL4A1 mutations cause cerebral small vessel disease by haploinsufficiency.
|
23065703 |
2013 |
rs1064795935
|
|
Movement Disorders
|
T |
0.700 |
GeneticVariation
|
CLINVAR |
Childhood presentation of COL4A1 mutations.
|
22574627 |
2012 |
rs1064795935
|
|
Movement Disorders
|
T |
0.700 |
GeneticVariation
|
CLINVAR |
COL4A1 mutations cause ocular dysgenesis, neuronal localization defects, and myopathy in mice and Walker-Warburg syndrome in humans.
|
21625620 |
2011 |
rs1064795935
|
|
Movement Disorders
|
T |
0.700 |
GeneticVariation
|
CLINVAR |
Cerebrovascular disease related to COL4A1 mutations in HANAC syndrome.
|
19949034 |
2009 |
rs1064795935
|
|
Movement Disorders
|
T |
0.700 |
GeneticVariation
|
CLINVAR |
COL4A1 mutation in preterm intraventricular hemorrhage.
|
19840616 |
2009 |
rs1064795935
|
|
Movement Disorders
|
T |
0.700 |
GeneticVariation
|
CLINVAR |
COL4A1 mutation in two preterm siblings with antenatal onset of parenchymal hemorrhage.
|
19194877 |
2009 |
rs1064795935
|
|
Movement Disorders
|
T |
0.700 |
GeneticVariation
|
CLINVAR |
COL4A1 mutation in Axenfeld-Rieger anomaly with leukoencephalopathy and stroke.
|
17696175 |
2007 |
rs1064795935
|
|
Movement Disorders
|
T |
0.700 |
GeneticVariation
|
CLINVAR |
Clinical and brain MRI follow-up study of a family with COL4A1 mutation.
|
17938367 |
2007 |
rs1064795935
|
|
Movement Disorders
|
T |
0.700 |
GeneticVariation
|
CLINVAR |
COL4A1 mutations and hereditary angiopathy, nephropathy, aneurysms, and muscle cramps.
|
18160688 |
2007 |
rs1064795935
|
|
Movement Disorders
|
T |
0.700 |
GeneticVariation
|
CLINVAR |
Role of COL4A1 in small-vessel disease and hemorrhagic stroke.
|
16598045 |
2006 |
rs1064795935
|
|
Movement Disorders
|
T |
0.700 |
GeneticVariation
|
CLINVAR |
Novel mutations in three families confirm a major role of COL4A1 in hereditary porencephaly.
|
16107487 |
2006 |
rs1064795935
|
|
Movement Disorders
|
T |
0.700 |
GeneticVariation
|
CLINVAR |
Neonatal porencephaly and adult stroke related to mutations in collagen IV A1.
|
16374828 |
2006 |
rs1064795935
|
|
Movement Disorders
|
T |
0.700 |
GeneticVariation
|
CLINVAR |
Mutations in Col4a1 cause perinatal cerebral hemorrhage and porencephaly.
|
15905400 |
2005 |
rs1064795935
|
|
Movement Disorders
|
T |
0.700 |
GeneticVariation
|
CLINVAR |
Autosomal-dominant familial hematuria with retinal arteriolar tortuosity and contractures: a novel syndrome.
|
15882279 |
2005 |
rs1064795935
|
|
Movement Disorders
|
T |
0.700 |
GeneticVariation
|
CLINVAR |
Hereditary infantile hemiparesis, retinal arteriolar tortuosity, and leukoencephalopathy.
|
12525718 |
2003 |
rs1064795935
|
|
Movement Disorders
|
T |
0.700 |
GeneticVariation
|
CLINVAR |
Familial porencephalic white matter disease in two generations.
|
6428250 |
1984 |