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This Concept Map, created with IHMC CmapTools, has information related to: CBL A1 Phenylketonuria, phenylalanine to tyrosine, large neutral amino acids (LNAA) decreases myelination, phenylalanine-free diet consists of decreased animal protein, glutamate in hippocampus, mutation in PAH gene, fetus causing phenylalanine embryo pathology, LNAA supplement competes w/ pheynylalanine, serum phenylalanine levels crosses placenta, placenta to fetus, serum phenylalanine levels is 500 mmol/L, 100% chance of baby being heterozygous may present w/ mild symptoms, phenylalanine embryo pathology including low birth weight, intellectual disability primarily in infants/ children, maintaing low serum phenylalanince levels to decrease chances of phenylalanine embryo pathology, pheynylalanine for sites on LAT-1 transporter, NT synthsesis causing intellectual disability, mild symptoms of PKU, PAH converts phenylalanine, myelination causing intellectual disability, PAH gene encodes PAH