rs199476104
|
|
Optic Atrophy, Hereditary, Leber
|
|
0.810 |
GeneticVariation
|
UNIPROT |
The mitochondrial ND6 gene is a hot spot for mutations that cause Leber's hereditary optic neuropathy.
|
11133798 |
2001 |
rs199476104
|
|
Optic Atrophy, Hereditary, Leber
|
|
0.810 |
GeneticVariation
|
UNIPROT |
Leber's hereditary optic neuropathy: clinical and molecular genetic findings in a patient with a new mutation in the ND6 gene.
|
10447650 |
1999 |
rs199476104
|
|
Optic Atrophy, Hereditary, Leber
|
|
0.810 |
GeneticVariation
|
UNIPROT |
Leber's hereditary optic neuropathy in Indonesia: two families with the mtDNA 11778G>A and 14484T>C mutations.
|
9452107 |
1998 |
rs199476104
|
|
Optic Atrophy, Hereditary, Leber
|
|
0.810 |
GeneticVariation
|
UNIPROT |
Leber's hereditary optic neuropathy: clinical and molecular genetic results obtained in a family with a new point mutation at nucleotide position 14498 in the ND 6 gene.
|
8854108 |
1996 |
rs199476104
|
|
Optic Atrophy, Hereditary, Leber
|
|
0.810 |
GeneticVariation
|
UNIPROT |
An ND-6 mitochondrial DNA mutation associated with Leber hereditary optic neuropathy.
|
1417830 |
1992 |
rs199476108
|
|
Optic Atrophy, Hereditary, Leber
|
|
0.810 |
GeneticVariation
|
UNIPROT |
The mitochondrial ND6 gene is a hot spot for mutations that cause Leber's hereditary optic neuropathy.
|
11133798 |
2001 |
rs199476108
|
|
Optic Atrophy, Hereditary, Leber
|
|
0.810 |
GeneticVariation
|
UNIPROT |
Leber's hereditary optic neuropathy: clinical and molecular genetic findings in a patient with a new mutation in the ND6 gene.
|
10447650 |
1999 |
rs199476108
|
|
Optic Atrophy, Hereditary, Leber
|
|
0.810 |
GeneticVariation
|
UNIPROT |
Leber's hereditary optic neuropathy in Indonesia: two families with the mtDNA 11778G>A and 14484T>C mutations.
|
9452107 |
1998 |
rs199476108
|
|
Optic Atrophy, Hereditary, Leber
|
|
0.810 |
GeneticVariation
|
UNIPROT |
Leber's hereditary optic neuropathy: clinical and molecular genetic results obtained in a family with a new point mutation at nucleotide position 14498 in the ND 6 gene.
|
8854108 |
1996 |
rs199476108
|
|
Optic Atrophy, Hereditary, Leber
|
|
0.810 |
GeneticVariation
|
UNIPROT |
An ND-6 mitochondrial DNA mutation associated with Leber hereditary optic neuropathy.
|
1417830 |
1992 |
rs199476105
|
|
LEBER OPTIC ATROPHY AND DYSTONIA
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Genetic and biochemical impairment of mitochondrial complex I activity in a family with Leber hereditary optic neuropathy and hereditary spastic dystonia.
|
8644732 |
1996 |
rs199476105
|
|
LEBER OPTIC ATROPHY AND DYSTONIA
|
|
0.800 |
GeneticVariation
|
UNIPROT |
A mitochondrial DNA mutation at nucleotide pair 14459 of the NADH dehydrogenase subunit 6 gene associated with maternally inherited Leber hereditary optic neuropathy and dystonia.
|
8016139 |
1994 |
rs199476106
|
|
Optic Atrophy, Hereditary, Leber
|
|
0.800 |
GeneticVariation
|
UNIPROT |
The mitochondrial ND6 gene is a hot spot for mutations that cause Leber's hereditary optic neuropathy.
|
11133798 |
2001 |
rs199476106
|
|
Optic Atrophy, Hereditary, Leber
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Leber's hereditary optic neuropathy: clinical and molecular genetic findings in a patient with a new mutation in the ND6 gene.
|
10447650 |
1999 |
rs199476106
|
|
Optic Atrophy, Hereditary, Leber
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Leber's hereditary optic neuropathy in Indonesia: two families with the mtDNA 11778G>A and 14484T>C mutations.
|
9452107 |
1998 |
rs199476106
|
|
Optic Atrophy, Hereditary, Leber
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Leber's hereditary optic neuropathy: clinical and molecular genetic results obtained in a family with a new point mutation at nucleotide position 14498 in the ND 6 gene.
|
8854108 |
1996 |
rs199476106
|
|
Optic Atrophy, Hereditary, Leber
|
|
0.800 |
GeneticVariation
|
UNIPROT |
An ND-6 mitochondrial DNA mutation associated with Leber hereditary optic neuropathy.
|
1417830 |
1992 |
rs199476107
|
|
MELAS Syndrome
|
|
0.800 |
GeneticVariation
|
UNIPROT |
An mtDNA mutation, 14453G-->A, in the NADH dehydrogenase subunit 6 associated with severe MELAS syndrome.
|
11781695 |
2001 |
rs199476109
|
|
Leigh Disease
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Impaired complex I assembly in a Leigh syndrome patient with a novel missense mutation in the ND6 gene.
|
14595656 |
2003 |
rs207459996
|
|
Colorectal Carcinoma
|
|
0.800 |
GeneticVariation
|
UNIPROT |
|
|
|
rs387906424
|
|
LEBER OPTIC ATROPHY AND DYSTONIA
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Genetic and biochemical impairment of mitochondrial complex I activity in a family with Leber hereditary optic neuropathy and hereditary spastic dystonia.
|
8644732 |
1996 |
rs387906424
|
|
LEBER OPTIC ATROPHY AND DYSTONIA
|
|
0.800 |
GeneticVariation
|
UNIPROT |
A mitochondrial DNA mutation at nucleotide pair 14459 of the NADH dehydrogenase subunit 6 gene associated with maternally inherited Leber hereditary optic neuropathy and dystonia.
|
8016139 |
1994 |
rs387906425
|
|
Optic Atrophy, Hereditary, Leber
|
|
0.800 |
GeneticVariation
|
UNIPROT |
The role of the ND5 gene in LHON: characterization of a new, heteroplasmic LHON mutation.
|
16240359 |
2005 |
rs387906425
|
|
Optic Atrophy, Hereditary, Leber
|
|
0.800 |
GeneticVariation
|
UNIPROT |
When does bilateral optic atrophy become Leber hereditary optic neuropathy?
|
8213825 |
1993 |
rs387906425
|
|
Optic Atrophy, Hereditary, Leber
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Mitochondrial DNA complex I and III mutations associated with Leber's hereditary optic neuropathy.
|
1732158 |
1992 |