Entrez Id: |
28976 |
Gene Symbol: |
ACAD9 |
ACAD9
|
0.610 |
AlteredExpression
|
disease |
BEFREE |
Complex I assembly function and fatty acid oxidation enzyme activity of ACAD9 both contribute to disease severity in ACAD9 deficiency.
|
25721401 |
2015 |
Entrez Id: |
28976 |
Gene Symbol: |
ACAD9 |
ACAD9
|
0.610 |
Biomarker
|
disease |
CTD_human |
|
|
|
Entrez Id: |
28976 |
Gene Symbol: |
ACAD9 |
ACAD9
|
0.610 |
GermlineCausalMutation
|
disease |
ORPHANET |
A new genetic disorder in mitochondrial fatty acid beta-oxidation: ACAD9 deficiency.
|
17564966 |
2007 |
Entrez Id: |
28976 |
Gene Symbol: |
ACAD9 |
ACAD9
|
0.610 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
Exome sequencing identifies ACAD9 mutations as a cause of complex I deficiency.
|
21057504 |
2010 |
Entrez Id: |
28976 |
Gene Symbol: |
ACAD9 |
ACAD9
|
0.610 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
Advantages and pitfalls of an extended gene panel for investigating complex neurometabolic phenotypes.
|
27604308 |
2016 |
Entrez Id: |
28976 |
Gene Symbol: |
ACAD9 |
ACAD9
|
0.610 |
Biomarker
|
disease |
CLINGEN |
Acyl-CoA dehydrogenase 9 (ACAD 9) is the long-chain acyl-CoA dehydrogenase in human embryonic and fetal brain.
|
16750164 |
2006 |
Entrez Id: |
28976 |
Gene Symbol: |
ACAD9 |
ACAD9
|
0.610 |
Biomarker
|
disease |
CLINGEN |
Human acyl-CoA dehydrogenase-9 plays a novel role in the mitochondrial beta-oxidation of unsaturated fatty acids.
|
16020546 |
2005 |
Entrez Id: |
28976 |
Gene Symbol: |
ACAD9 |
ACAD9
|
0.610 |
Biomarker
|
disease |
CLINGEN |
High incidence and variable clinical outcome of cardiac hypertrophy due to ACAD9 mutations in childhood.
|
26669660 |
2016 |
Entrez Id: |
28976 |
Gene Symbol: |
ACAD9 |
ACAD9
|
0.610 |
Biomarker
|
disease |
CLINGEN |
Complex I assembly function and fatty acid oxidation enzyme activity of ACAD9 both contribute to disease severity in ACAD9 deficiency.
|
25721401 |
2015 |
Entrez Id: |
28976 |
Gene Symbol: |
ACAD9 |
ACAD9
|
0.610 |
Biomarker
|
disease |
CLINGEN |
A new genetic disorder in mitochondrial fatty acid beta-oxidation: ACAD9 deficiency.
|
17564966 |
2007 |
Entrez Id: |
28976 |
Gene Symbol: |
ACAD9 |
ACAD9
|
0.610 |
Biomarker
|
disease |
CLINGEN |
Molecular diagnosis in mitochondrial complex I deficiency using exome sequencing.
|
22499348 |
2012 |
Entrez Id: |
28976 |
Gene Symbol: |
ACAD9 |
ACAD9
|
0.610 |
Biomarker
|
disease |
CLINGEN |
Cloning and functional characterization of ACAD-9, a novel member of human acyl-CoA dehydrogenase family.
|
12359260 |
2002 |
Entrez Id: |
28976 |
Gene Symbol: |
ACAD9 |
ACAD9
|
0.610 |
Biomarker
|
disease |
CLINGEN |
Exome sequencing identifies ACAD9 mutations as a cause of complex I deficiency.
|
21057504 |
2010 |
Entrez Id: |
28976 |
Gene Symbol: |
ACAD9 |
ACAD9
|
0.610 |
Biomarker
|
disease |
CLINGEN |
Acyl-CoA dehydrogenase 9 is required for the biogenesis of oxidative phosphorylation complex I.
|
20816094 |
2010 |