Mesh : Amino Acid Transport Systems, Acidic / deficiency genetics Antiporters / deficiency genetics Brain Stem / abnormalities pathology Child Child, Preschool DNA Copy Number Variations Discoidin Domain Receptors Hereditary Central Nervous System Demyelinating Diseases / diagnosis genetics Humans Image Processing, Computer-Assisted Infant Magnetic Resonance Imaging Male Microarray Analysis Mitochondrial Diseases / diagnosis genetics Mutation Myelin Proteolipid Protein / genetics Osteochondrodysplasias / diagnosis genetics Pelizaeus-Merzbacher Disease / diagnosis genetics Psychomotor Disorders / diagnosis genetics Receptor Protein-Tyrosine Kinases / genetics Receptors, Mitogen / genetics
来 源:
DOI:10.1002/ajmg.a.35686
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