rs267606899
|
|
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 |
rs267606899
|
|
Optic Atrophy, Hereditary, Leber
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Mitochondrial DNA complex I and III mutations associated with Leber's hereditary optic neuropathy.
|
1732158 |
1992 |
rs267606899
|
|
Optic Atrophy, Hereditary, Leber
|
|
0.800 |
GeneticVariation
|
UNIPROT |
When does bilateral optic atrophy become Leber hereditary optic neuropathy?
|
8213825 |
1993 |
rs267606899
|
|
Optic Atrophy, Hereditary, Leber
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Alternative, simultaneous complex I mitochondrial DNA mutations in Leber's hereditary optic neuropathy.
|
1900003 |
1991 |
rs267606898
|
|
MELAS Syndrome
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Mutations in the ND5 subunit of complex I of the mitochondrial DNA are a frequent cause of oxidative phosphorylation disease.
|
17400793 |
2007 |
rs267606898
|
|
MELAS Syndrome
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Is the mitochondrial complex I ND5 gene a hot-spot for MELAS causing mutations?
|
12509858 |
2003 |
rs267606898
|
|
MELAS Syndrome
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Novel mitochondrial DNA ND5 mutation in a patient with clinical features of MELAS and MERRF.
|
15767514 |
2005 |
rs267606898
|
|
MELAS Syndrome
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Identification of a novel mutation in the mtDNA ND5 gene associated with MELAS.
|
9299505 |
1997 |
rs267606897
|
|
MELAS Syndrome
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Identification of a novel mutation in the mtDNA ND5 gene associated with MELAS.
|
9299505 |
1997 |
rs267606897
|
|
MELAS Syndrome
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Mutations in the ND5 subunit of complex I of the mitochondrial DNA are a frequent cause of oxidative phosphorylation disease.
|
17400793 |
2007 |
rs267606897
|
|
MELAS Syndrome
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Is the mitochondrial complex I ND5 gene a hot-spot for MELAS causing mutations?
|
12509858 |
2003 |
rs267606897
|
|
MELAS Syndrome
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Novel mitochondrial DNA ND5 mutation in a patient with clinical features of MELAS and MERRF.
|
15767514 |
2005 |
rs267606895
|
|
MELAS Syndrome
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Mutations in the ND5 subunit of complex I of the mitochondrial DNA are a frequent cause of oxidative phosphorylation disease.
|
17400793 |
2007 |
rs267606895
|
|
MELAS Syndrome
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Identification of a novel mutation in the mtDNA ND5 gene associated with MELAS.
|
9299505 |
1997 |
rs267606895
|
|
MELAS Syndrome
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Novel mitochondrial DNA ND5 mutation in a patient with clinical features of MELAS and MERRF.
|
15767514 |
2005 |
rs267606895
|
|
MELAS Syndrome
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Is the mitochondrial complex I ND5 gene a hot-spot for MELAS causing mutations?
|
12509858 |
2003 |
rs267606894
|
|
MELAS Syndrome
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Mutations in the ND5 subunit of complex I of the mitochondrial DNA are a frequent cause of oxidative phosphorylation disease.
|
17400793 |
2007 |
rs267606894
|
|
MELAS Syndrome
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Identification of a novel mutation in the mtDNA ND5 gene associated with MELAS.
|
9299505 |
1997 |
rs267606894
|
|
MELAS Syndrome
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Is the mitochondrial complex I ND5 gene a hot-spot for MELAS causing mutations?
|
12509858 |
2003 |
rs267606894
|
|
MELAS Syndrome
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Novel mitochondrial DNA ND5 mutation in a patient with clinical features of MELAS and MERRF.
|
15767514 |
2005 |
rs267606893
|
|
Leigh Disease
|
|
0.800 |
GeneticVariation
|
UNIPROT |
A missense mutation in the mitochondrial ND5 gene associated with a Leigh-MELAS overlap syndrome.
|
12796552 |
2003 |
rs267606893
|
|
Leigh Disease
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Leigh disease associated with a novel mitochondrial DNA ND5 mutation.
|
11938446 |
2002 |
rs267606893
|
|
Leigh Disease
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Mutations in the ND5 subunit of complex I of the mitochondrial DNA are a frequent cause of oxidative phosphorylation disease.
|
17400793 |
2007 |
rs267606892
|
|
Colorectal Carcinoma
|
|
0.800 |
GeneticVariation
|
UNIPROT |
|
|
|
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 |