rs137852886
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
A novel missense mutation in the glycogen branching enzyme gene in a child with myopathy and hepatopathy.
|
10545044 |
1999 |
rs137852886
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Hepatic and neuromuscular forms of glycogen storage disease type IV caused by mutations in the same glycogen-branching enzyme gene.
|
8613547 |
1996 |
rs137852886
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Clinical and genetic heterogeneity of branching enzyme deficiency (glycogenosis type IV).
|
15452297 |
2004 |
rs137852887
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
A novel missense mutation in the glycogen branching enzyme gene in a child with myopathy and hepatopathy.
|
10545044 |
1999 |
rs137852887
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Hepatic and neuromuscular forms of glycogen storage disease type IV caused by mutations in the same glycogen-branching enzyme gene.
|
8613547 |
1996 |
rs137852887
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Clinical and genetic heterogeneity of branching enzyme deficiency (glycogenosis type IV).
|
15452297 |
2004 |
rs137852889
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Hepatic and neuromuscular forms of glycogen storage disease type IV caused by mutations in the same glycogen-branching enzyme gene.
|
8613547 |
1996 |
rs137852889
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Clinical and genetic heterogeneity of branching enzyme deficiency (glycogenosis type IV).
|
15452297 |
2004 |
rs137852889
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
A novel missense mutation in the glycogen branching enzyme gene in a child with myopathy and hepatopathy.
|
10545044 |
1999 |
rs137852891
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Clinical and genetic heterogeneity of branching enzyme deficiency (glycogenosis type IV).
|
15452297 |
2004 |
rs137852891
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
A novel missense mutation in the glycogen branching enzyme gene in a child with myopathy and hepatopathy.
|
10545044 |
1999 |
rs137852891
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Hepatic and neuromuscular forms of glycogen storage disease type IV caused by mutations in the same glycogen-branching enzyme gene.
|
8613547 |
1996 |