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Peroxisomal Disorders
Gerald Raymond
Department of Pediatrics
Research output
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Chapter in Book/Report/Conference proceeding
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Keyphrases
Peroxisomal Disorders
100%
DNA Analysis
50%
Adulthood
50%
Seizure
50%
Nervous System
50%
Biogenesis
50%
Multisystem
50%
Developmental Abnormality
50%
Biochemical Measures
50%
Measurement Analysis
50%
Common Disease
50%
Neuronal Migration
50%
Peroxisome
50%
Subcellular Organelles
50%
Multi-enzyme
50%
Demyelination
50%
Neurological Manifestations
50%
Biochemical Abnormalities
50%
X-linked Adrenoleukodystrophy (X-ALD)
50%
Neuroscience
Peroxisome
100%
Peroxisomal Disorder
100%
Nervous System
50%
Neuronal Migration
50%
Adrenoleukodystrophy
50%
Biochemistry, Genetics and Molecular Biology
Biogenesis
100%
Peroxisome
100%
DNA Analysis
50%
Inborn Error of Metabolism
50%
Adrenoleukodystrophy
50%