Entrez Id: |
54902 |
Gene Symbol: |
TTC19 |
TTC19
|
Leigh Disease
|
0.300 |
Biomarker |
CLINGEN |
Novel Homozygous Variant in TTC19 Causing Mitochondrial Complex III Deficiency with Recurrent Stroke-Like Episodes: Expanding the Phenotype.
|
29961508 |
2018 |
Entrez Id: |
54902 |
Gene Symbol: |
TTC19 |
TTC19
|
Leigh Disease
|
0.300 |
Biomarker |
CLINGEN |
TTC19 Plays a Husbandry Role on UQCRFS1 Turnover in the Biogenesis of Mitochondrial Respiratory Complex III.
|
28673544 |
2017 |
Entrez Id: |
54902 |
Gene Symbol: |
TTC19 |
TTC19
|
Leigh Disease
|
0.300 |
Biomarker |
CLINGEN |
Mutations in TTC19: expanding the molecular, clinical and biochemical phenotype.
|
25887401 |
2015 |
Entrez Id: |
54902 |
Gene Symbol: |
TTC19 |
TTC19
|
Leigh Disease
|
0.300 |
Biomarker |
CLINGEN |
Proteomics. Tissue-based map of the human proteome.
|
25613900 |
2015 |
Entrez Id: |
54902 |
Gene Symbol: |
TTC19 |
TTC19
|
Leigh Disease
|
0.300 |
Biomarker |
CLINGEN |
Exome sequencing reveals a novel TTC19 mutation in an autosomal recessive spinocerebellar ataxia patient.
|
24397319 |
2014 |
Entrez Id: |
54902 |
Gene Symbol: |
TTC19 |
TTC19
|
Leigh Disease
|
0.300 |
Biomarker |
CLINGEN |
Mutations in TTC19 cause mitochondrial complex III deficiency and neurological impairment in humans and flies.
|
21278747 |
2011 |
Entrez Id: |
54902 |
Gene Symbol: |
TTC19 |
TTC19
|
Leigh Disease
|
0.300 |
Biomarker |
CLINGEN |
Mitochondrial Complex III Deficiency Caused by TTC19 Defects: Report of a Novel Mutation and Review of Literature.
|
25772319 |
2015 |
Entrez Id: |
54902 |
Gene Symbol: |
TTC19 |
TTC19
|
Leigh Disease
|
0.300 |
Biomarker |
CLINGEN |
A novel mutation in TTC19 associated with isolated complex III deficiency, cerebellar hypoplasia, and bilateral basal ganglia lesions.
|
25452764 |
2014 |
Entrez Id: |
54902 |
Gene Symbol: |
TTC19 |
TTC19
|
LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY
|
0.300 |
Biomarker |
CLINGEN |
Mitochondrial Complex III Deficiency Caused by TTC19 Defects: Report of a Novel Mutation and Review of Literature.
|
25772319 |
2015 |
Entrez Id: |
54902 |
Gene Symbol: |
TTC19 |
TTC19
|
LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY
|
0.300 |
Biomarker |
CLINGEN |
Novel Homozygous Variant in TTC19 Causing Mitochondrial Complex III Deficiency with Recurrent Stroke-Like Episodes: Expanding the Phenotype.
|
29961508 |
2018 |
Entrez Id: |
54902 |
Gene Symbol: |
TTC19 |
TTC19
|
LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY
|
0.300 |
Biomarker |
CLINGEN |
Exome sequencing reveals a novel TTC19 mutation in an autosomal recessive spinocerebellar ataxia patient.
|
24397319 |
2014 |
Entrez Id: |
54902 |
Gene Symbol: |
TTC19 |
TTC19
|
LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY
|
0.300 |
Biomarker |
CLINGEN |
Mutations in TTC19 cause mitochondrial complex III deficiency and neurological impairment in humans and flies.
|
21278747 |
2011 |
Entrez Id: |
54902 |
Gene Symbol: |
TTC19 |
TTC19
|
LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY
|
0.300 |
Biomarker |
CLINGEN |
Proteomics. Tissue-based map of the human proteome.
|
25613900 |
2015 |
Entrez Id: |
54902 |
Gene Symbol: |
TTC19 |
TTC19
|
LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY
|
0.300 |
Biomarker |
CLINGEN |
TTC19 Plays a Husbandry Role on UQCRFS1 Turnover in the Biogenesis of Mitochondrial Respiratory Complex III.
|
28673544 |
2017 |
Entrez Id: |
54902 |
Gene Symbol: |
TTC19 |
TTC19
|
LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY
|
0.300 |
Biomarker |
CLINGEN |
A novel mutation in TTC19 associated with isolated complex III deficiency, cerebellar hypoplasia, and bilateral basal ganglia lesions.
|
25452764 |
2014 |
Entrez Id: |
54902 |
Gene Symbol: |
TTC19 |
TTC19
|
LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY
|
0.300 |
Biomarker |
CLINGEN |
Mutations in TTC19: expanding the molecular, clinical and biochemical phenotype.
|
25887401 |
2015 |
Entrez Id: |
54902 |
Gene Symbol: |
TTC19 |
TTC19
|
Leigh Syndrome Due To Mitochondrial Complex II Deficiency
|
0.300 |
Biomarker |
CLINGEN |
TTC19 Plays a Husbandry Role on UQCRFS1 Turnover in the Biogenesis of Mitochondrial Respiratory Complex III.
|
28673544 |
2017 |
Entrez Id: |
54902 |
Gene Symbol: |
TTC19 |
TTC19
|
Leigh Syndrome Due To Mitochondrial Complex II Deficiency
|
0.300 |
Biomarker |
CLINGEN |
Mutations in TTC19: expanding the molecular, clinical and biochemical phenotype.
|
25887401 |
2015 |
Entrez Id: |
54902 |
Gene Symbol: |
TTC19 |
TTC19
|
Leigh Syndrome Due To Mitochondrial Complex II Deficiency
|
0.300 |
Biomarker |
CLINGEN |
Novel Homozygous Variant in TTC19 Causing Mitochondrial Complex III Deficiency with Recurrent Stroke-Like Episodes: Expanding the Phenotype.
|
29961508 |
2018 |
Entrez Id: |
54902 |
Gene Symbol: |
TTC19 |
TTC19
|
Leigh Syndrome Due To Mitochondrial Complex II Deficiency
|
0.300 |
Biomarker |
CLINGEN |
Mitochondrial Complex III Deficiency Caused by TTC19 Defects: Report of a Novel Mutation and Review of Literature.
|
25772319 |
2015 |
Entrez Id: |
54902 |
Gene Symbol: |
TTC19 |
TTC19
|
Leigh Syndrome Due To Mitochondrial Complex II Deficiency
|
0.300 |
Biomarker |
CLINGEN |
Exome sequencing reveals a novel TTC19 mutation in an autosomal recessive spinocerebellar ataxia patient.
|
24397319 |
2014 |
Entrez Id: |
54902 |
Gene Symbol: |
TTC19 |
TTC19
|
Leigh Syndrome Due To Mitochondrial Complex II Deficiency
|
0.300 |
Biomarker |
CLINGEN |
A novel mutation in TTC19 associated with isolated complex III deficiency, cerebellar hypoplasia, and bilateral basal ganglia lesions.
|
25452764 |
2014 |
Entrez Id: |
54902 |
Gene Symbol: |
TTC19 |
TTC19
|
Leigh Syndrome Due To Mitochondrial Complex II Deficiency
|
0.300 |
Biomarker |
CLINGEN |
Mutations in TTC19 cause mitochondrial complex III deficiency and neurological impairment in humans and flies.
|
21278747 |
2011 |
Entrez Id: |
54902 |
Gene Symbol: |
TTC19 |
TTC19
|
Leigh Syndrome Due To Mitochondrial Complex II Deficiency
|
0.300 |
Biomarker |
CLINGEN |
Proteomics. Tissue-based map of the human proteome.
|
25613900 |
2015 |
Entrez Id: |
54902 |
Gene Symbol: |
TTC19 |
TTC19
|
Leigh Syndrome due to Mitochondrial Complex III Deficiency
|
0.300 |
Biomarker |
CLINGEN |
Mutations in TTC19 cause mitochondrial complex III deficiency and neurological impairment in humans and flies.
|
21278747 |
2011 |