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ACAD9 gene
Known as:
ACAD9
, acyl-CoA dehydrogenase family member 9
, MGC14452
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National Institutes of Health
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Related topics
Related topics
1 relation
acyl-CoA dehydrogenase
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Etudes structurales de la protéine ACAD9 et des facteurs d'assemblage du complexe 1 de la chaîne respiratoire mitochondriale pour établir leur implication dans les processus neurodégénératifs
R. Bouverot
2019
Corpus ID: 182875556
Les mitochondries sont en charge de la bioenergetique cellulaire, tout particulierement dans le cerveau humain, au sein duquel…
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2017
2017
Lifetime exercise intolerance with lactic acidosis as key manifestation of novel compound heterozygous ACAD9 mutations causing complex I deficiency
B. Schrank
,
B. Schoser
,
+5 authors
S. Augustis
Neuromuscular Disorders
2017
Corpus ID: 3460935
2017
2017
Assembly defects of multiple respiratory chain complexes in a child with cardiac hypertrophy associated with a novel ACAD9 mutation.
K. Fragaki
,
A. Chaussenot
,
+4 authors
V. Paquis-Flucklinger
Molecular Genetics and Metabolism
2017
Corpus ID: 3985463
Review
2016
Review
2016
An atypical presentation of ACAD9 deficiency: Diagnosis by whole exome sequencing broadens the phenotypic spectrum and alters treatment approach
H. Aintablian
,
V. Narayanan
,
N. Belnap
,
K. Ramsey
,
T. Grebe
Molecular Genetics and Metabolism Reports
2016
Corpus ID: 8648949
2015
2015
Another "Complex" Case: Complex I Deficiency Secondary to Acyl-CoA Dehydrogenase 9 Mutation.
Rod C. Daniel
,
Manmeet Singh
,
K. OʼRourke
American Journal of the Medical Sciences
2015
Corpus ID: 21833178
A 15-year-old, 69 2 99, athletic Caucasian male who was previously healthy presented to the hospital with acute myalgia 1 day…
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Review
2010
Review
2010
Cell Metabolism Previews Assembling Complex I with ACAD 9
I. Scheffler
2010
Corpus ID: 207759691
Mitochondrial diseases due to partial deficiencies in themitochondrial oxidative phosphorylation system have been recognized for…
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