rs104894270
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Molecular diagnosis in mitochondrial complex I deficiency using exome sequencing.
|
22499348 |
2012 |
rs104894270
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
A Novel NDUFS3 mutation in a Chinese patient with severe Leigh syndrome.
|
30140060 |
2018 |
rs104894270
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Mutant NDUFS3 subunit of mitochondrial complex I causes Leigh syndrome.
|
14729820 |
2004 |
rs28939714
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Mutant NDUFS3 subunit of mitochondrial complex I causes Leigh syndrome.
|
14729820 |
2004 |
rs28939714
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Molecular diagnosis in mitochondrial complex I deficiency using exome sequencing.
|
22499348 |
2012 |
rs28939714
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
A Novel NDUFS3 mutation in a Chinese patient with severe Leigh syndrome.
|
30140060 |
2018 |
rs142248674
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
A Novel NDUFS3 mutation in a Chinese patient with severe Leigh syndrome.
|
30140060 |
2018 |
rs142248674
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Mutant NDUFS3 subunit of mitochondrial complex I causes Leigh syndrome.
|
14729820 |
2004 |
rs142248674
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Molecular diagnosis in mitochondrial complex I deficiency using exome sequencing.
|
22499348 |
2012 |
rs104894270
|
|
T |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs104894270
|
|
T |
0.800 |
GeneticVariation |
CLINVAR |
Mutant NDUFS3 subunit of mitochondrial complex I causes Leigh syndrome.
|
14729820 |
2004 |
rs104894270
|
|
T |
0.800 |
GeneticVariation |
CLINVAR |
A Novel NDUFS3 mutation in a Chinese patient with severe Leigh syndrome.
|
30140060 |
2018 |
rs104894270
|
|
T |
0.800 |
GeneticVariation |
CLINVAR |
Molecular diagnosis in mitochondrial complex I deficiency using exome sequencing.
|
22499348 |
2012 |
rs28939714
|
|
T |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs28939714
|
|
T |
0.800 |
GeneticVariation |
CLINVAR |
Mutant NDUFS3 subunit of mitochondrial complex I causes Leigh syndrome.
|
14729820 |
2004 |