rs369586696
|
|
|
0.710 |
GeneticVariation |
UNIPROT |
Here we report two novel ALDOB variants (p.R46W and p.Y343H) and an intragenic deletion that we found in patients with suspected HFI.
|
20848650 |
2010 |
rs369586696
|
|
|
0.710 |
GeneticVariation |
BEFREE |
Here we report two novel ALDOB variants (p.R46W and p.Y343H) and an intragenic deletion that we found in patients with suspected HFI.
|
20848650 |
2010 |
rs369586696
|
|
|
0.710 |
GeneticVariation |
UNIPROT |
The spectrum of aldolase B (ALDOB) mutations and the prevalence of hereditary fructose intolerance in Central Europe.
|
15880727 |
2005 |
rs369586696
|
|
|
0.710 |
GeneticVariation |
UNIPROT |
Six novel alleles identified in Italian hereditary fructose intolerance patients enlarge the mutation spectrum of the aldolase B gene.
|
15532022 |
2004 |
rs369586696
|
|
|
0.710 |
GeneticVariation |
UNIPROT |
Molecular analysis of the aldolase B gene in patients with hereditary fructose intolerance from Spain.
|
12205126 |
2002 |
rs369586696
|
|
|
0.710 |
GeneticVariation |
UNIPROT |
Functional and molecular modelling studies of two hereditary fructose intolerance-causing mutations at arginine 303 in human liver aldolase.
|
10970798 |
2000 |
rs369586696
|
|
|
0.710 |
GeneticVariation |
UNIPROT |
Screening for hereditary fructose intolerance mutations by reverse dot-blot.
|
10024431 |
1999 |
rs369586696
|
|
|
0.710 |
GeneticVariation |
UNIPROT |
Identification of a novel mutation (Leu 256-->Pro) in the human aldolase B gene associated with hereditary fructose intolerance.
|
8162030 |
1994 |
rs369586696
|
|
|
0.710 |
GeneticVariation |
UNIPROT |
A partially active mutant aldolase B from a patient with hereditary fructose intolerance.
|
8299883 |
1994 |
rs369586696
|
|
|
0.710 |
GeneticVariation |
UNIPROT |
A new aldolase B variant, N334K, is a common cause of hereditary fructose intolerance in Yugoslavia.
|
2336380 |
1990 |
rs369586696
|
|
|
0.710 |
GeneticVariation |
UNIPROT |
Molecular analysis of aldolase B genes in hereditary fructose intolerance.
|
1967768 |
1990 |
rs369586696
|
|
|
0.710 |
GeneticVariation |
UNIPROT |
Catalytic deficiency of human aldolase B in hereditary fructose intolerance caused by a common missense mutation.
|
3383242 |
1988 |