Biochemistry, Genetics and Molecular Biology
Oxidoreductase
100%
Dehydrogenase
100%
Missense Mutation
100%
Coenzyme A
100%
Single-Nucleotide Polymorphism
50%
Wild Type
50%
Allele
50%
Liquid
50%
Amino Acids
50%
Prevalence
50%
Cofactor
50%
Western Blot
50%
Single Nucleotide Polymorphism
50%
Splice Site Mutation
50%
Metabolic Disorder
50%
Catalysis
50%
Thioesterase
50%
Mitochondrial Matrix
50%
Standing
50%
Electrophoresis
50%
Keyphrases
ETHE1
100%
Ethylmalonic Encephalopathy
100%
Dehydrogenase
18%
Acyl-coenzyme A
18%
Missense mutation
18%
Short Chain
18%
Etiology
9%
Single nucleotide Polymorphism
9%
Early Onset
9%
Frameshift
9%
Amino Acid Residues
9%
SNP Analysis
9%
Western Blot Analysis
9%
Acidemia
9%
Two Dimensional
9%
Splicing mutation
9%
Metabolic Disorders
9%
Pathogenic Role
9%
Catalytic Function
9%
Three Dimensional Model
9%
Experiment-based
9%
Body Fluids
9%
Orthotics
9%
Homodimeric
9%
Mitochondrial Matrix
9%
Methylmalonic Acidemia
9%
Petechiae
9%
Progressive Encephalopathy
9%
Thioesterase
9%
Ethylmalonic Acid
9%
Blue Native Electrophoresis
9%
Acrocyanosis
9%