Keyphrases
Retinal Degeneration
100%
ACO2
100%
Mitochondrial Aconitase
100%
Retina
40%
Cerebellum
40%
Aconitase
40%
Lymphoblast
40%
Neurodegenerative Diseases
20%
Cerebellar Atrophy
20%
Brain MRI
20%
Psychomotor Retardation
20%
Carbohydrates
20%
Clinical Spectrum
20%
6 Months of Age
20%
Krebs Cycle
20%
Homozygosity Mapping
20%
Corpus Callosum
20%
Whole Exome Sequencing
20%
Glutamate
20%
Lysosomal Storage Disease
20%
Cortical Atrophy
20%
Neuroaxonal Dystrophy
20%
Individual-based
20%
Developmental Milestones
20%
Dysmyelination
20%
Non-invasive Biomarkers
20%
Mitochondrial Respiratory Chain
20%
Cerebrum
20%
Restrictive Conditions
20%
Hypotonia
20%
Laboratory Investigation
20%
ACO1
20%
Retinal Atrophy
20%
Optic Nerve Atrophy
20%
Deletion Strain
20%
Respiratory Chain Deficiency
20%
Ophthalmic Abnormalities
20%
Skeletal muscle Mitochondria
20%
Athetosis
20%
Progressive Visual Loss
20%
Seizure Disorder
20%
Failure to Acquire
20%
N-glycosylation Defects
20%
Medicine and Dentistry
Retina Degeneration
100%
Aconitase
100%
Disease
40%
Cerebellum
40%
Lymphoblast
40%
Biological Marker
20%
Homozygosity
20%
Epileptic Seizure
20%
Psychomotor Retardation
20%
Magnetic Resonance Imaging of Brain
20%
Cerebellum Atrophy
20%
Visual Impairment
20%
Lysosomal Storage Disease
20%
Developmental Milestone
20%
Exome Sequencing
20%
Respiratory Chain
20%
Corpus Callosum
20%
Optic Nerve
20%
Glutamic Acid
20%
Infancy
20%
Myelin Deficiency
20%
Neurodegenerative Disorder
20%
Glycosylation
20%
Storage Disease
20%
Citric Acid Cycle
20%
Hypotonia
20%
Huperzine A
20%
Athetosis
20%
Mitochondrial Disorder
20%
Infantile Neuroaxonal Dystrophy
20%
Muscle Mitochondrion
20%
Neuroscience
Aconitate Hydratase
100%
Retinal Degeneration
100%
Cerebellum
40%
Lymphoblast
40%
Neurodegenerative Disorder
20%
Glutamic Acid
20%
Psychomotor Retardation
20%
Magnetic Resonance Imaging of Brain
20%
Mitochondrion
20%
Corpus Callosum
20%
Optic Nerve
20%
Exome Sequencing
20%
Electron Transport Chain
20%
Citric Acid Cycle
20%
Cerebrum
20%
Hypotonia
20%
Athetosis
20%
Epilepsy
20%
Glycosylation
20%
Pharmacology, Toxicology and Pharmaceutical Science
Retina Degeneration
100%
Aconitase
100%
Disease
60%
Glutamic Acid
20%
Biological Marker
20%
Visual Impairment
20%
Muscle Hypotonia
20%
Storage Disease
20%
Cerebellum Atrophy
20%
Lysosome Storage Disease
20%
Athetosis
20%
Neuroaxonal Dystrophy
20%
Psychomotor Retardation
20%
Myelin Deficiency
20%
Huperzine A
20%
Biochemistry, Genetics and Molecular Biology
Aconitase
100%
Lymphoblast
40%
Mitochondrion
20%
Wild Type
20%
Glycosylation
20%
Exome Sequencing
20%
Homozygosity
20%
Citric Acid Cycle
20%
Infancy
20%
Electron Transport Chain
20%
Mitochondrial Disorder
20%
Krebs Cycle
20%
Glutamic Acid
20%