rs121909533
|
|
G |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs121909534
|
|
A |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs121909533
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Human aldolase A deficiency associated with a hemolytic anemia: thermolabile aldolase due to a single base mutation.
|
2825199 |
1987 |
rs121909534
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Human aldolase A deficiency associated with a hemolytic anemia: thermolabile aldolase due to a single base mutation.
|
2825199 |
1987 |
rs138824667
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Human aldolase A deficiency associated with a hemolytic anemia: thermolabile aldolase due to a single base mutation.
|
2825199 |
1987 |
rs121909533
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Human aldolase A of a hemolytic anemia patient with Asp-128----Gly substitution: characteristics of an enzyme generated in E. coli transfected with the expression plasmid pHAAD128G.
|
2229018 |
1990 |
rs121909534
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Human aldolase A of a hemolytic anemia patient with Asp-128----Gly substitution: characteristics of an enzyme generated in E. coli transfected with the expression plasmid pHAAD128G.
|
2229018 |
1990 |
rs138824667
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Human aldolase A of a hemolytic anemia patient with Asp-128----Gly substitution: characteristics of an enzyme generated in E. coli transfected with the expression plasmid pHAAD128G.
|
2229018 |
1990 |
rs121909533
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Brief report: inherited metabolic myopathy and hemolysis due to a mutation in aldolase A.
|
8598869 |
1996 |
rs121909534
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Brief report: inherited metabolic myopathy and hemolysis due to a mutation in aldolase A.
|
8598869 |
1996 |
rs138824667
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Brief report: inherited metabolic myopathy and hemolysis due to a mutation in aldolase A.
|
8598869 |
1996 |
rs121909533
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Human aldolase A natural mutants: relationship between flexibility of the C-terminal region and enzyme function.
|
14766013 |
2004 |
rs121909533
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Hemolytic anemia and severe rhabdomyolysis caused by compound heterozygous mutations of the gene for erythrocyte/muscle isozyme of aldolase, ALDOA(Arg303X/Cys338Tyr).
|
14615364 |
2004 |
rs121909534
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Hemolytic anemia and severe rhabdomyolysis caused by compound heterozygous mutations of the gene for erythrocyte/muscle isozyme of aldolase, ALDOA(Arg303X/Cys338Tyr).
|
14615364 |
2004 |
rs121909534
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Human aldolase A natural mutants: relationship between flexibility of the C-terminal region and enzyme function.
|
14766013 |
2004 |
rs138824667
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Human aldolase A natural mutants: relationship between flexibility of the C-terminal region and enzyme function.
|
14766013 |
2004 |
rs138824667
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Hemolytic anemia and severe rhabdomyolysis caused by compound heterozygous mutations of the gene for erythrocyte/muscle isozyme of aldolase, ALDOA(Arg303X/Cys338Tyr).
|
14615364 |
2004 |